Linked Data
ClinVar Variation Id:
2718230
ClinVar RCV Id:
RCV003551086
MyVariant Identifiers:
chr12:g.121435422C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120997619C>T , CM000674.2:g.120997619C>T | GRCh38 |
| NC_000012.11:g.121435422C>T , CM000674.1:g.121435422C>T | GRCh37 |
| NC_000012.10:g.119919805C>T | NCBI36 |
| NG_011731.2:g.23874C>T , LRG_522:g.23874C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.*202C>T | ENSP00000453965.2:n.*202C>T | |
| ENST00000257555.11:c.1455C>T MANE Select | ENSP00000257555.5:p.Thr485= | |
| ENST00000257555.10:c.1455C>T | ENSP00000257555.4:p.Thr485= | |
| ENST00000400024.6:c.1455C>T | ENSP00000476181.1:p.Thr485= | |
| ENST00000402929.5:n.2321C>T | ||
| ENST00000535955.5:n.171C>T | ||
| ENST00000538626.2:n.319C>T | ||
| ENST00000538646.5:c.*431C>T | ENSP00000443964.1:n.*431C>T | |
| ENST00000540108.1:c.*895C>T | ENSP00000445445.1:n.*895C>T | |
| ENST00000541395.5:c.1455C>T | ENSP00000443112.1:p.Thr485= | |
| ENST00000541924.5:c.*469C>T | ENSP00000440361.1:n.*469C>T | |
| ENST00000543255.1:n.499C>T | ||
| ENST00000543427.5:c.918C>T | ENSP00000439721.2:p.Thr306= | |
| ENST00000544413.2:c.1455C>T | ENSP00000438804.1:p.Thr485= | |
| ENST00000544574.5:c.*218C>T | ENSP00000438565.1:n.*218C>T | |
| ENST00000560968.5:c.1272C>T | ||
| ENST00000615446.4:c.243C>T | ENSP00000483994.1:p.Thr81= | |
| ENST00000617366.4:c.587-15C>T | ENSP00000481967.1:n.587-15C>T | |
| NM_000545.5:c.1455C>T , LRG_522t1:c.1455C>T | NP_000536.5:p.Thr485= | |
| NM_000545.6:c.1455C>T | NP_000536.5:p.Thr485= | |
| NM_001306179.1:c.1455C>T | NP_001293108.1:p.Thr485= | |
| XM_005253931.2:c.1455C>T | XP_005253988.1:p.Thr485= | |
| XM_024449168.1:c.1455C>T | XP_024304936.1:p.Thr485= | |
| NM_000545.8:c.1455C>T MANE Select | NP_000536.6:p.Thr485= | |
| NM_001306179.2:c.1455C>T | NP_001293108.2:p.Thr485= |