Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6695995C= , CM000666.2:g.6695995C= | GRCh38 |
| NC_000004.11:g.6697722C= , CM000666.1:g.6697722C= | GRCh37 |
| NC_000004.10:g.6748623C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296370.4:c.139-898C= MANE Select | ENSP00000296370.3:n.139-898C= | |
| ENST00000296370.3:c.139-898C= | ENSP00000296370.3:n.139-898C= | |
| ENST00000513778.1:n.36-898C= | ||
| NM_005980.2:c.139-898C= | NP_005971.1:n.139-898C= | |
| NM_005980.3:c.139-898C= MANE Select | NP_005971.1:n.139-898C= |