Linked Data
dbSNP Id:
rs1782398029
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17339713G>A , CM000669.2:g.17339713G>A | GRCh38 |
| NC_000007.13:g.17379337G>A , CM000669.1:g.17379337G>A | GRCh37 |
| NC_000007.12:g.17345862G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242057.9:c.1888G>A MANE Select | ENSP00000242057.4:p.Val630Ile | |
| ENST00000637807.1:c.1858G>A | ENSP00000490530.1:p.Val620Ile | |
| ENST00000642825.1:c.1843G>A | ENSP00000495987.1:p.Val615Ile | |
| ENST00000242057.8:c.1888G>A | ENSP00000242057.4:p.Val630Ile | |
| ENST00000463496.1:c.1888G>A | ENSP00000436466.1:p.Val630Ile | |
| NM_001621.4:c.1888G>A | NP_001612.1:p.Val630Ile | |
| NM_001621.5:c.1888G>A MANE Select | NP_001612.1:p.Val630Ile |