Linked Data
ClinVar Variation Id:
1774654
ClinVar RCV Id:
RCV002402990
dbSNP Id:
rs1230187187
gnomAD v2:
7-21856189-C-T
gnomAD v4:
7-21816571-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21816571C>T , CM000669.2:g.21816571C>T | GRCh38 |
| NC_000007.13:g.21856189C>T , CM000669.1:g.21856189C>T | GRCh37 |
| NC_000007.12:g.21822714C>T | NCBI36 |
| NG_012886.2:g.278357C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.10437C>T MANE Select | ENSP00000475939.1:p.Ser3479= | |
| ENST00000328843.10:c.10458C>T | ENSP00000330671.7:p.Ser3486= | |
| ENST00000409508.7:c.10437C>T | ENSP00000475939.1:p.Ser3479= | |
| ENST00000620169.4:c.10458C>T | ENSP00000481693.1:p.Ser3486= | |
| NM_001277115.1:c.10437C>T | NP_001264044.1:p.Ser3479= | |
| NM_001277115.2:c.10437C>T MANE Select | NP_001264044.1:p.Ser3479= |