Linked Data
ClinVar Variation Id:
1119554
ClinVar RCV Id:
RCV001449023
dbSNP Id:
rs2102713648
MyVariant Identifiers:
chr1:g.215901606G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215728264G>A , CM000663.2:g.215728264G>A | GRCh38 |
| NC_000001.10:g.215901606G>A , CM000663.1:g.215901606G>A | GRCh37 |
| NC_000001.9:g.213968229G>A | NCBI36 |
| NG_009497.1:g.700133C>T | |
| NG_009497.2:g.700185C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11832C>T MANE Select | ENSP00000305941.3:p.Ala3944= | |
| ENST00000674083.1:c.11832C>T | ENSP00000501296.1:p.Ala3944= | |
| ENST00000307340.7:c.11832C>T | ENSP00000305941.3:p.Ala3944= | |
| NM_206933.2:c.11832C>T | NP_996816.2:p.Ala3944= | |
| NM_206933.3:c.11832C>T | NP_996816.2:p.Ala3944= | |
| NM_206933.4:c.11832C>T MANE Select | NP_996816.3:p.Ala3944= |