Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.41475664C= , CM000667.2:g.41475664C= | GRCh38 |
| NC_000005.9:g.41475766C= , CM000667.1:g.41475766C= | GRCh37 |
| NC_000005.8:g.41511523C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001005473.3:c.103+34760G= MANE Select | NP_001005473.1:n.103+34760G= |
| ENST00000377801.8:c.103+34760G= MANE Select | ENSP00000367032.3:n.103+34760G= |
| NM_001005473.2:c.103+34760G= | NP_001005473.1:n.103+34760G= |
| ENST00000328457.5:c.103+34760G= | ENSP00000333751.3:n.103+34760G= |
| ENST00000377801.7:c.103+34760G= | ENSP00000367032.3:n.103+34760G= |