Linked Data
dbSNP Id:
rs2069937128
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951850G>A , CM000670.2:g.19951850G>A | GRCh38 |
| NC_000008.10:g.19809361G>A , CM000670.1:g.19809361G>A | GRCh37 |
| NC_000008.9:g.19853641G>A | NCBI36 |
| NG_008855.1:g.17780G>A | |
| NG_008855.2:g.55134G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.331G>A MANE Select | ENSP00000497642.1:p.Val111Met | |
| ENST00000311322.8:c.331G>A | ENSP00000309757.6:p.Val111Met | |
| ENST00000520959.5:c.103G>A | ENSP00000428496.1:p.Val35Met | |
| ENST00000524029.5:c.331G>A | ENSP00000428237.1:p.Val111Met | |
| NM_000237.2:c.331G>A | NP_000228.1:p.Val111Met | |
| NM_000237.3:c.331G>A MANE Select | NP_000228.1:p.Val111Met |