Linked Data
dbSNP Id:
rs750008138
gnomAD v4:
22-42128871-G-A
MyVariant Identifiers:
chr22:g.42524873G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42128871G>A , CM000684.2:g.42128871G>A | GRCh38 |
| NC_000022.10:g.42524873G>A , CM000684.1:g.42524873G>A | GRCh37 |
| NC_000022.9:g.40854817G>A | NCBI36 |
| NG_008376.3:g.6121C>T | |
| NG_008376.4:g.6940C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360124.10:c.426C>T | ENSP00000353241.6:p.Arg142= | |
| ENST00000645361.2:c.579C>T MANE Select | ENSP00000496150.1:p.Arg193= | |
| ENST00000359033.4:c.426C>T | ENSP00000351927.4:p.Arg142= | |
| ENST00000360124.9:c.246C>T | ENSP00000353241.5:p.Arg82= | |
| ENST00000360608.9:c.579C>T | ENSP00000353820.5:p.Arg193= | |
| ENST00000389970.7:c.513C>T | ENSP00000374620.4:p.Arg171= | |
| ENST00000488442.1:n.1303C>T | ||
| NM_000106.5:c.579C>T | NP_000097.3:p.Arg193= | |
| NM_001025161.2:c.426C>T | NP_001020332.2:p.Arg142= | |
| XM_011529966.1:c.579C>T | XP_011528268.1:p.Arg193= | |
| XM_011529967.1:c.579C>T | XP_011528269.1:p.Arg193= | |
| XM_011529968.1:c.579C>T | XP_011528270.1:p.Arg193= | |
| XM_011529969.1:c.435C>T | XP_011528271.1:p.Arg145= | |
| XM_011529970.1:c.426C>T | XP_011528272.1:p.Arg142= | |
| XM_011529971.1:c.435C>T | XP_011528273.1:p.Arg145= | |
| XM_011529972.1:c.579C>T | XP_011528274.1:p.Arg193= | |
| NM_000106.6:c.579C>T MANE Select | NP_000097.3:p.Arg193= | |
| NM_001025161.3:c.426C>T | NP_001020332.2:p.Arg142= |