Linked Data
dbSNP Id:
rs1373677424
gnomAD v2:
16-67470030-G-A
gnomAD v3:
16-67436127-G-A
gnomAD v4:
16-67436127-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436127G>A , CM000678.2:g.67436127G>A | GRCh38 |
| NC_000016.9:g.67470030G>A , CM000678.1:g.67470030G>A | GRCh37 |
| NC_000016.8:g.66027531G>A | NCBI36 |
| NG_011482.1:g.50060C>T | |
| NG_016549.1:g.9995G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.649G>A MANE Select | ENSP00000316786.5:p.Val217Met | |
| ENST00000326152.5:c.649G>A | ENSP00000316786.5:p.Val217Met | |
| ENST00000566606.1:c.627G>A | ENSP00000473429.1:n.627G>A | |
| ENST00000567684.2:n.512G>A | ||
| NM_000196.3:c.649G>A | NP_000187.3:p.Val217Met | |
| NM_000196.4:c.649G>A MANE Select | NP_000187.3:p.Val217Met |