Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73998280T= , CM000666.2:g.73998280T= | GRCh38 |
| NC_000004.11:g.74863997T= , CM000666.1:g.74863997T= | GRCh37 |
| NC_000004.10:g.75082861T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296027.5:c.168A= MANE Select | ENSP00000296027.4:p.Gln56= | |
| ENST00000296027.4:c.168A= | ENSP00000296027.4:p.Gln56= | |
| NM_002994.4:c.168A= | NP_002985.1:p.Gln56= | |
| NM_002994.5:c.168A= MANE Select | NP_002985.1:p.Gln56= |