Linked Data
ClinVar Variation Id:
1381182
ClinVar RCV Id:
RCV001895234
dbSNP Id:
rs12073994
ExAC:
1:215953273 G / T
gnomAD v2:
1-215953273-G-T
gnomAD v3:
1-215779931-G-T
gnomAD v4:
1-215779931-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215779931G>T , CM000663.2:g.215779931G>T | GRCh38 |
| NC_000001.10:g.215953273G>T , CM000663.1:g.215953273G>T | GRCh37 |
| NC_000001.9:g.214019896G>T | NCBI36 |
| NG_009497.1:g.648466C>A | |
| NG_009497.2:g.648518C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10851C>A MANE Select | ENSP00000305941.3:p.Asn3617Lys | |
| ENST00000674083.1:c.10851C>A | ENSP00000501296.1:p.Asn3617Lys | |
| ENST00000307340.7:c.10851C>A | ENSP00000305941.3:p.Asn3617Lys | |
| NM_206933.2:c.10851C>A | NP_996816.2:p.Asn3617Lys | |
| NM_206933.3:c.10851C>A | NP_996816.2:p.Asn3617Lys | |
| NM_206933.4:c.10851C>A MANE Select | NP_996816.3:p.Asn3617Lys |