Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.22033044G= , CM000685.2:g.22033044G= | GRCh38 |
| NC_000023.10:g.22051162G= , CM000685.1:g.22051162G= | GRCh37 |
| NC_000023.9:g.21961083G= | NCBI36 |
| NG_007563.2:g.5242G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475778.2:n.465G= | ||
| ENST00000683214.1:n.465G= | ||
| ENST00000684143.1:c.39G= | ENSP00000508264.1:p.Lys13= | |
| ENST00000379374.5:c.39G= MANE Select | ENSP00000368682.4:p.Lys13= | |
| ENST00000379374.4:c.39G= | ENSP00000368682.4:p.Lys13= | |
| NM_000444.5:c.39G= | NP_000435.3:p.Lys13= | |
| NM_001282754.1:c.39G= | NP_001269683.1:p.Lys13= | |
| XM_011545535.1:c.39G= | XP_011543837.1:p.Lys13= | |
| XR_001755695.1:n.718G= | ||
| NM_000444.6:c.39G= MANE Select | NP_000435.3:p.Lys13= | |
| NM_001282754.2:c.39G= | NP_001269683.1:p.Lys13= |