Linked Data
dbSNP Id:
rs554886125
ExAC:
16:223497 C / A
gnomAD v2:
16-223497-C-A
gnomAD v3:
16-173498-C-A
gnomAD v4:
16-173498-C-A
COSMIC:
COSM3278739
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173498C>A , CM000678.2:g.173498C>A | GRCh38 |
| NC_000016.9:g.223497C>A , CM000678.1:g.223497C>A | GRCh37 |
| NC_000016.8:g.163497C>A | NCBI36 |
| NG_000006.1:g.34361C>A | |
| NG_059186.1:g.1848C>A | |
| NG_059271.1:g.5652C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000251595.11:c.327C>A MANE Select | ENSP00000251595.6:p.Thr109= | |
| ENST00000251595.10:c.327C>A | ENSP00000251595.6:p.Thr109= | |
| ENST00000397806.1:c.231C>A | ENSP00000380908.1:p.Thr77= | |
| ENST00000482565.1:n.463C>A | ||
| NM_000517.4:c.327C>A | NP_000508.1:p.Thr109= | |
| NM_000517.6:c.327C>A MANE Select | NP_000508.1:p.Thr109= |