Linked Data
dbSNP Id:
rs761895610
ExAC:
22:42524818 C / T
gnomAD v2:
22-42524818-C-T
gnomAD v3:
22-42128816-C-T
gnomAD v4:
22-42128816-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42128816C>T , CM000684.2:g.42128816C>T | GRCh38 |
| NC_000022.10:g.42524818C>T , CM000684.1:g.42524818C>T | GRCh37 |
| NC_000022.9:g.40854762C>T | NCBI36 |
| NG_008376.3:g.6176G>A | |
| NG_008376.4:g.6995G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360124.10:c.481G>A | ENSP00000353241.6:p.Gly161Arg | |
| ENST00000645361.2:c.634G>A MANE Select | ENSP00000496150.1:p.Gly212Arg | |
| ENST00000359033.4:c.481G>A | ENSP00000351927.4:p.Gly161Arg | |
| ENST00000360124.9:c.301G>A | ENSP00000353241.5:p.Gly101Arg | |
| ENST00000360608.9:c.634G>A | ENSP00000353820.5:p.Gly212Arg | |
| ENST00000389970.7:c.568G>A | ENSP00000374620.4:p.Gly190Arg | |
| ENST00000488442.1:n.1358G>A | ||
| NM_000106.5:c.634G>A | NP_000097.3:p.Gly212Arg | |
| NM_001025161.2:c.481G>A | NP_001020332.2:p.Gly161Arg | |
| XM_011529966.1:c.634G>A | XP_011528268.1:p.Gly212Arg | |
| XM_011529967.1:c.634G>A | XP_011528269.1:p.Gly212Arg | |
| XM_011529968.1:c.634G>A | XP_011528270.1:p.Gly212Arg | |
| XM_011529969.1:c.490G>A | XP_011528271.1:p.Gly164Arg | |
| XM_011529970.1:c.481G>A | XP_011528272.1:p.Gly161Arg | |
| XM_011529971.1:c.490G>A | XP_011528273.1:p.Gly164Arg | |
| XM_011529972.1:c.634G>A | XP_011528274.1:p.Gly212Arg | |
| NM_000106.6:c.634G>A MANE Select | NP_000097.3:p.Gly212Arg | |
| NM_001025161.3:c.481G>A | NP_001020332.2:p.Gly161Arg |