Linked Data
gnomAD v4:
1-186166907-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186166907G>A , CM000663.2:g.186166907G>A | GRCh38 |
| NC_000001.10:g.186136039G>A , CM000663.1:g.186136039G>A | GRCh37 |
| NC_000001.9:g.184402662G>A | NCBI36 |
| NG_011841.1:g.437357G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.15539G>A MANE Select | ENSP00000271588.4:p.Gly5180Asp | |
| ENST00000271588.8:c.15539G>A | ENSP00000271588.4:p.Gly5180Asp | |
| ENST00000475585.1:n.163-4430G>A | ||
| NM_031935.2:c.15539G>A | NP_114141.2:p.Gly5180Asp | |
| XM_011510037.1:c.15254G>A | XP_011508339.1:p.Gly5085Asp | |
| XM_011510038.1:c.15539G>A | XP_011508340.1:p.Gly5180Asp | |
| XM_011510038.3:c.15539G>A | XP_011508340.1:p.Gly5180Asp | |
| XM_017002437.1:c.13562G>A | XP_016857926.1:p.Gly4521Asp | |
| NM_031935.3:c.15539G>A MANE Select | NP_114141.2:p.Gly5180Asp |