Linked Data
ClinVar Variation Id:
30063
dbSNP Id:
rs143153871
ExAC:
7:152345927 G / A
gnomAD v2:
7-152345927-G-A
gnomAD v3:
7-152648842-G-A
gnomAD v4:
7-152648842-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648842G>A , CM000669.2:g.152648842G>A | GRCh38 |
| NC_000007.13:g.152345927G>A , CM000669.1:g.152345927G>A | GRCh37 |
| NC_000007.12:g.151976860G>A | NCBI36 |
| NG_027988.1:g.32324C>T | |
| NG_027988.2:g.32324C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698506.1:c.475C>T | ENSP00000513758.1:p.Arg159Ter | |
| ENST00000359321.2:c.643C>T MANE Select | ENSP00000352271.1:p.Arg215Ter | |
| ENST00000359321.1:c.643C>T | ENSP00000352271.1:p.Arg215Ter | |
| ENST00000495707.1:n.665C>T | ||
| NM_005431.1:c.643C>T | NP_005422.1:p.Arg215Ter | |
| NM_005431.2:c.643C>T MANE Select | NP_005422.1:p.Arg215Ter |