Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154835C= , CM000668.2:g.3154835C= | GRCh38 |
| NC_000006.11:g.3155069C= , CM000668.1:g.3155069C= | GRCh37 |
| NC_000006.10:g.3100068C= | NCBI36 |
| NG_042223.1:g.7715G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.366G= MANE Select | ENSP00000369703.2:p.Lys122= | |
| ENST00000679400.1:n.422G= | ||
| ENST00000679907.1:n.754G= | ||
| ENST00000680036.1:n.1148G= | ||
| ENST00000680967.1:n.1456G= | ||
| ENST00000333628.3:c.366G= | ENSP00000369703.2:p.Lys122= | |
| ENST00000489942.1:n.561G= | ||
| NM_001069.2:c.366G= | NP_001060.1:p.Lys122= | |
| NM_001310315.1:c.111G= | NP_001297244.1:p.Lys37= | |
| NM_001069.3:c.366G= MANE Select | NP_001060.1:p.Lys122= | |
| NM_001310315.2:c.111G= | NP_001297244.1:p.Lys37= |