Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956390G= , CM000670.2:g.24956390G= | GRCh38 |
| NC_000008.10:g.24813904G= , CM000670.1:g.24813904G= | GRCh37 |
| NC_000008.9:g.24869821G= | NCBI36 |
| NG_008492.1:g.5228C= , LRG_259:g.5228C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.2:c.126C= MANE Select | ENSP00000482169.2:p.Ser42= | |
| ENST00000610854.1:c.126C= | ENSP00000482169.1:p.Ser42= | |
| ENST00000615973.1:n.332C= | ||
| ENST00000619417.1:c.126C= | ENSP00000483690.1:p.Ser42= | |
| NM_006158.4:c.126C= , LRG_259t1:c.126C= | NP_006149.2:p.Ser42= | |
| NM_006158.5:c.126C= MANE Select | NP_006149.2:p.Ser42= |