Linked Data
dbSNP Id:
rs565013903
ExAC:
22:42524213 C / T
gnomAD v2:
22-42524213-C-T
gnomAD v3:
22-42128211-C-T
gnomAD v4:
22-42128211-C-T
MyVariant Identifiers:
chr22:g.42524213C>T (hg19)
chr22:g.42524213_42524214delinsTG (hg19)
chr22:g.42128211C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42128211C>T , CM000684.2:g.42128211C>T | GRCh38 |
| NC_000022.10:g.42524213C>T , CM000684.1:g.42524213C>T | GRCh37 |
| NC_000022.9:g.40854157C>T | NCBI36 |
| NG_008376.3:g.6781G>A | |
| NG_008376.4:g.7600G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360124.10:c.653G>A | ENSP00000353241.6:p.Arg218Gln | |
| ENST00000645361.2:c.806G>A MANE Select | ENSP00000496150.1:p.Arg269Gln | |
| ENST00000359033.4:c.653G>A | ENSP00000351927.4:p.Arg218Gln | |
| ENST00000360124.9:c.473G>A | ENSP00000353241.5:p.Arg158Gln | |
| ENST00000360608.9:c.806G>A | ENSP00000353820.5:p.Arg269Gln | |
| ENST00000389970.7:c.740G>A | ENSP00000374620.4:p.Arg247Gln | |
| ENST00000488442.1:n.1530G>A | ||
| NM_000106.5:c.806G>A | NP_000097.3:p.Arg269Gln | |
| NM_001025161.2:c.653G>A | NP_001020332.2:p.Arg218Gln | |
| XM_011529966.1:c.806G>A | XP_011528268.1:p.Arg269Gln | |
| XM_011529967.1:c.806G>A | XP_011528269.1:p.Arg269Gln | |
| XM_011529968.1:c.806G>A | XP_011528270.1:p.Arg269Gln | |
| XM_011529969.1:c.662G>A | XP_011528271.1:p.Arg221Gln | |
| XM_011529970.1:c.653G>A | XP_011528272.1:p.Arg218Gln | |
| XM_011529971.1:c.662G>A | XP_011528273.1:p.Arg221Gln | |
| XM_011529972.1:c.806G>A | XP_011528274.1:p.Arg269Gln | |
| NM_000106.6:c.806G>A MANE Select | NP_000097.3:p.Arg269Gln | |
| NM_001025161.3:c.653G>A | NP_001020332.2:p.Arg218Gln |