Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956070G= , CM000670.2:g.24956070G= | GRCh38 |
| NC_000008.10:g.24813584G= , CM000670.1:g.24813584G= | GRCh37 |
| NC_000008.9:g.24869501G= | NCBI36 |
| NG_008492.1:g.5548C= , LRG_259:g.5548C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006158.5:c.446C= MANE Select | NP_006149.2:p.Ala149= |
| ENST00000610854.2:c.446C= MANE Select | ENSP00000482169.2:p.Ala149= |
| NM_006158.4:c.446C= , LRG_259t1:c.446C= | NP_006149.2:p.Ala149= |
| ENST00000610854.1:c.446C= | ENSP00000482169.1:p.Ala149= |
| ENST00000615973.1:n.652C= | |
| ENST00000619417.1:c.446C= | ENSP00000483690.1:p.Ala149= |