Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55105679G= , CM000666.2:g.55105679G= | GRCh38 |
| NC_000004.11:g.55971846G= , CM000666.1:g.55971846G= | GRCh37 |
| NC_000004.10:g.55666603G= | NCBI36 |
| NG_012004.1:g.24917C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002253.4:c.1645+153C= MANE Select | NP_002244.1:n.1645+153C= |
| ENST00000263923.5:c.1645+153C= MANE Select | ENSP00000263923.4:n.1645+153C= |
| NM_002253.2:c.1645+153C= | NP_002244.1:n.1645+153C= |
| NM_002253.3:c.1645+153C= | NP_002244.1:n.1645+153C= |
| ENST00000263923.4:c.1645+153C= | ENSP00000263923.4:n.1645+153C= |
| ENST00000512566.1:n.1645+153C= | |
| ENST00000647068.1:n.1658+153C= |