Linked Data
MyVariant Identifiers:
chr1:g.182555390C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.182586255C>T , CM000663.2:g.182586255C>T | GRCh38 |
| NC_000001.10:g.182555390C>T , CM000663.1:g.182555390C>T | GRCh37 |
| NC_000001.9:g.180822013C>T | NCBI36 |
| NG_009024.2:g.5719G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367559.7:c.552G>A MANE Select | ENSP00000356530.3:p.Leu184= | |
| ENST00000539397.1:c.552G>A | ENSP00000440844.1:p.Leu184= | |
| NM_021133.3:c.552G>A | NP_066956.1:p.Leu184= | |
| XM_005245411.2:c.552G>A | XP_005245468.1:p.Leu184= | |
| XR_001737359.1:n.835G>A | ||
| XR_001737360.1:n.835G>A | ||
| NM_021133.4:c.552G>A MANE Select | NP_066956.1:p.Leu184= |