Linked Data
ClinVar Variation Id:
1107669
ClinVar RCV Id:
RCV001432909
dbSNP Id:
rs766042296
ExAC:
1:215901624 G / A
gnomAD v2:
1-215901624-G-A
gnomAD v4:
1-215728282-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215728282G>A , CM000663.2:g.215728282G>A | GRCh38 |
| NC_000001.10:g.215901624G>A , CM000663.1:g.215901624G>A | GRCh37 |
| NC_000001.9:g.213968247G>A | NCBI36 |
| NG_009497.1:g.700115C>T | |
| NG_009497.2:g.700167C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11814C>T MANE Select | ENSP00000305941.3:p.Tyr3938= | |
| ENST00000674083.1:c.11814C>T | ENSP00000501296.1:p.Tyr3938= | |
| ENST00000307340.7:c.11814C>T | ENSP00000305941.3:p.Tyr3938= | |
| NM_206933.2:c.11814C>T | NP_996816.2:p.Tyr3938= | |
| NM_206933.3:c.11814C>T | NP_996816.2:p.Tyr3938= | |
| NM_206933.4:c.11814C>T MANE Select | NP_996816.3:p.Tyr3938= |