Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100045505C= , CM000672.2:g.100045505C= | GRCh38 |
| NC_000010.10:g.101805262C= , CM000672.1:g.101805262C= | GRCh37 |
| NC_000010.9:g.101795252C= | NCBI36 |
| NG_012060.1:g.41381G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370418.8:c.1231-2932G= MANE Select | ENSP00000359446.3:n.1231-2932G= | |
| ENST00000370418.7:c.1231-2932G= | ENSP00000359446.3:n.1231-2932G= | |
| NM_001308.2:c.1231-2932G= | NP_001299.1:n.1231-2932G= | |
| XM_011539299.1:c.1273-2932G= | XP_011537601.1:n.1273-2932G= | |
| NM_001308.3:c.1231-2932G= MANE Select | NP_001299.1:n.1231-2932G= |