Linked Data
ClinVar Variation Id:
1161372
ClinVar RCV Id:
RCV001505850
dbSNP Id:
rs777691425
gnomAD v2:
7-21639644-C-T
gnomAD v4:
7-21600026-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21600026C>T , CM000669.2:g.21600026C>T | GRCh38 |
| NC_000007.13:g.21639644C>T , CM000669.1:g.21639644C>T | GRCh37 |
| NC_000007.12:g.21606169C>T | NCBI36 |
| NG_012886.2:g.61812C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.2907C>T MANE Select | ENSP00000475939.1:p.Phe969= | |
| ENST00000328843.10:c.2907C>T | ENSP00000330671.7:p.Phe969= | |
| ENST00000409508.7:c.2907C>T | ENSP00000475939.1:p.Phe969= | |
| ENST00000620169.4:c.2907C>T | ENSP00000481693.1:p.Phe969= | |
| NM_001277115.1:c.2907C>T | NP_001264044.1:p.Phe969= | |
| NM_001277115.2:c.2907C>T MANE Select | NP_001264044.1:p.Phe969= |