Linked Data
dbSNP Id:
rs763998727
ExAC:
20:948661 C / A
gnomAD v2:
20-948661-C-A
gnomAD v4:
20-968018-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.968018C>A , CM000682.2:g.968018C>A | GRCh38 |
| NC_000020.10:g.948661C>A , CM000682.1:g.948661C>A | GRCh37 |
| NC_000020.9:g.896661C>A | NCBI36 |
| NG_013043.1:g.39247G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217260.9:c.200G>T MANE Select | ENSP00000217260.4:p.Gly67Val | |
| ENST00000217260.8:c.200G>T | ENSP00000217260.4:p.Gly67Val | |
| ENST00000400634.2:c.200G>T | ENSP00000383475.2:p.Gly67Val | |
| NM_001029871.3:c.200G>T | NP_001025042.2:p.Gly67Val | |
| NM_001040007.2:c.200G>T | NP_001035096.1:p.Gly67Val | |
| XM_011529232.1:c.248G>T | XP_011527534.1:p.Gly83Val | |
| XM_011529233.1:c.248G>T | XP_011527535.1:p.Gly83Val | |
| XR_937068.1:n.320G>T | ||
| XR_937069.1:n.315G>T | ||
| XM_017027839.1:c.200G>T | XP_016883328.1:p.Gly67Val | |
| NM_001029871.4:c.200G>T MANE Select | NP_001025042.2:p.Gly67Val | |
| NM_001040007.3:c.200G>T | NP_001035096.1:p.Gly67Val |