Linked Data
dbSNP Id:
rs745850264
ExAC:
22:36960839 G / T
gnomAD v2:
22-36960839-G-T
gnomAD v3:
22-36564792-G-T
gnomAD v4:
22-36564792-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564792G>T , CM000684.2:g.36564792G>T | GRCh38 |
| NC_000022.10:g.36960839G>T , CM000684.1:g.36960839G>T | GRCh37 |
| NC_000022.9:g.35290785G>T | NCBI36 |
| NG_031861.1:g.142852C>A | |
| NG_031861.2:g.143067C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.531C>A MANE Select | ENSP00000300105.6:p.Gly177= | |
| ENST00000300105.6:c.531C>A | ENSP00000300105.6:p.Gly177= | |
| NM_006078.3:c.531C>A | NP_006069.1:p.Gly177= | |
| NM_006078.4:c.531C>A | NP_006069.1:p.Gly177= | |
| XM_017028531.2:c.273C>A | XP_016884020.1:p.Gly91= | |
| NM_001379051.1:c.462C>A | NP_001365980.1:p.Gly154= | |
| NM_006078.5:c.531C>A MANE Select | NP_006069.1:p.Gly177= | |
| NR_166440.1:n.1897C>A |