Linked Data
ClinVar Variation Id:
2719310
ClinVar RCV Id:
RCV003537827
dbSNP Id:
rs953927007
gnomAD v2:
7-21675613-C-T
gnomAD v4:
7-21635995-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21635995C>T , CM000669.2:g.21635995C>T | GRCh38 |
| NC_000007.13:g.21675613C>T , CM000669.1:g.21675613C>T | GRCh37 |
| NC_000007.12:g.21642138C>T | NCBI36 |
| NG_012886.2:g.97781C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.4625C>T MANE Select | ENSP00000475939.1:p.Thr1542Ile | |
| ENST00000328843.10:c.4640C>T | ENSP00000330671.7:p.Thr1547Ile | |
| ENST00000409508.7:c.4625C>T | ENSP00000475939.1:p.Thr1542Ile | |
| ENST00000465593.1:n.651C>T | ||
| ENST00000620169.4:c.4640C>T | ENSP00000481693.1:p.Thr1547Ile | |
| NM_001277115.1:c.4625C>T | NP_001264044.1:p.Thr1542Ile | |
| NM_001277115.2:c.4625C>T MANE Select | NP_001264044.1:p.Thr1542Ile |