Linked Data
dbSNP Id:
rs779492927
ExAC:
22:42524876 C / T
gnomAD v2:
22-42524876-C-T
gnomAD v3:
22-42128874-C-T
gnomAD v4:
22-42128874-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42128874C>T , CM000684.2:g.42128874C>T | GRCh38 |
| NC_000022.10:g.42524876C>T , CM000684.1:g.42524876C>T | GRCh37 |
| NC_000022.9:g.40854820C>T | NCBI36 |
| NG_008376.3:g.6118G>A | |
| NG_008376.4:g.6937G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360124.10:c.423G>A | ENSP00000353241.6:p.Gly141= | |
| ENST00000645361.2:c.576G>A MANE Select | ENSP00000496150.1:p.Gly192= | |
| ENST00000359033.4:c.423G>A | ENSP00000351927.4:p.Gly141= | |
| ENST00000360124.9:c.243G>A | ENSP00000353241.5:p.Gly81= | |
| ENST00000360608.9:c.576G>A | ENSP00000353820.5:p.Gly192= | |
| ENST00000389970.7:c.510G>A | ENSP00000374620.4:p.Gly170= | |
| ENST00000488442.1:n.1300G>A | ||
| NM_000106.5:c.576G>A | NP_000097.3:p.Gly192= | |
| NM_001025161.2:c.423G>A | NP_001020332.2:p.Gly141= | |
| XM_011529966.1:c.576G>A | XP_011528268.1:p.Gly192= | |
| XM_011529967.1:c.576G>A | XP_011528269.1:p.Gly192= | |
| XM_011529968.1:c.576G>A | XP_011528270.1:p.Gly192= | |
| XM_011529969.1:c.432G>A | XP_011528271.1:p.Gly144= | |
| XM_011529970.1:c.423G>A | XP_011528272.1:p.Gly141= | |
| XM_011529971.1:c.432G>A | XP_011528273.1:p.Gly144= | |
| XM_011529972.1:c.576G>A | XP_011528274.1:p.Gly192= | |
| NM_000106.6:c.576G>A MANE Select | NP_000097.3:p.Gly192= | |
| NM_001025161.3:c.423G>A | NP_001020332.2:p.Gly141= |