Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18175134G= , CM000681.2:g.18175134G= | GRCh38 |
| NC_000019.9:g.18285944G= , CM000681.1:g.18285944G= | GRCh37 |
| NC_000019.8:g.18146944G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006332.5:c.227G= MANE Select | NP_006323.2:p.Arg76= |
| ENST00000407280.4:c.227G= MANE Select | ENSP00000384886.1:p.Arg76= |
| NM_006332.4:c.227G= | NP_006323.2:p.Arg76= |
| ENST00000407280.3:c.227G= | ENSP00000384886.1:p.Arg76= |
| ENST00000593731.1:c.*1663G= | ENSP00000471914.1:n.*1663G= |
| ENST00000597802.2:c.227G= | ENSP00000470527.2:p.Arg76= |
| ENST00000600463.1:n.966G= |