Linked Data
MyVariant Identifiers:
chr1:g.154543917G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571441G>A , CM000663.2:g.154571441G>A | GRCh38 |
| NC_000001.10:g.154543917G>A , CM000663.1:g.154543917G>A | GRCh37 |
| NC_000001.9:g.152810541G>A | NCBI36 |
| NG_008027.1:g.8661G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.618G>A MANE Select | ENSP00000357461.3:p.Val206= | |
| ENST00000636034.1:c.618G>A | ENSP00000489703.1:p.Val206= | |
| ENST00000637900.1:c.624G>A | ENSP00000490474.1:p.Val208= | |
| ENST00000368476.3:c.618G>A | ENSP00000357461.3:p.Val206= | |
| NM_000748.2:c.618G>A | NP_000739.1:p.Val206= | |
| XM_017000180.2:c.108G>A | XP_016855669.1:p.Val36= | |
| XR_001736952.2:n.870G>A | ||
| NM_000748.3:c.618G>A MANE Select | NP_000739.1:p.Val206= |