Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56453658C>T , CM000674.2:g.56453658C>T | GRCh38 |
| NC_000012.11:g.56847442C>T , CM000674.1:g.56847442C>T | GRCh37 |
| NC_000012.10:g.55133709C>T | NCBI36 |
| NG_021397.1:g.5994G>A | |
| NG_021397.2:g.20509G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648304.1:c.*82G>A | ENSP00000497190.1:n.*82G>A | |
| ENST00000648442.1:n.591G>A | ||
| ENST00000650166.1:n.347G>A | ||
| ENST00000652304.1:c.458G>A MANE Select | ENSP00000498622.1:p.Arg153Gln | |
| ENST00000257979.4:c.458G>A | ENSP00000257979.4:p.Arg153Gln | |
| ENST00000555551.1:n.414G>A | ||
| NM_012064.3:c.458G>A | NP_036196.1:p.Arg153Gln | |
| XM_011538354.1:c.173G>A | XP_011536656.1:p.Arg58Gln | |
| NM_012064.4:c.458G>A MANE Select | NP_036196.1:p.Arg153Gln | |
| XM_017019306.1:c.101G>A | XP_016874795.1:p.Arg34Gln |