Linked Data
gnomAD v4:
1-17348036-C-A
COSMIC:
COSM6459669
MyVariant Identifiers:
chr1:g.17674531C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17348036C>A , CM000663.2:g.17348036C>A | GRCh38 |
| NC_000001.10:g.17674531C>A , CM000663.1:g.17674531C>A | GRCh37 |
| NC_000001.9:g.17547118C>A | NCBI36 |
| NG_023261.2:g.44847C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.1143C>A MANE Select | ENSP00000364597.4:p.Ile381= | |
| ENST00000468945.1:n.202C>A | ||
| ENST00000487048.5:n.110C>A | ||
| NM_012387.2:c.1143C>A | NP_036519.2:p.Ile381= | |
| XM_011541150.1:c.957C>A | XP_011539452.1:p.Ile319= | |
| XM_011541151.1:c.1143C>A | XP_011539453.1:p.Ile381= | |
| XM_011541152.1:c.606C>A | XP_011539454.1:p.Ile202= | |
| XM_011541153.1:c.1143C>A | XP_011539455.1:p.Ile381= | |
| XM_011541154.1:c.1143C>A | XP_011539456.1:p.Ile381= | |
| XM_011541155.1:c.1143C>A | XP_011539457.1:p.Ile381= | |
| XM_011541156.1:c.1143C>A | XP_011539458.1:p.Ile381= | |
| XM_011541157.1:c.252C>A | XP_011539459.1:p.Ile84= | |
| XM_011541154.2:c.1143C>A | XP_011539456.1:p.Ile381= | |
| NM_012387.3:c.1143C>A MANE Select | NP_036519.2:p.Ile381= |