Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94981609C= , CM000672.2:g.94981609C= | GRCh38 |
| NC_000010.10:g.96741366C= , CM000672.1:g.96741366C= | GRCh37 |
| NC_000010.9:g.96731356C= | NCBI36 |
| NG_008385.1:g.47952C= | |
| NG_008385.2:g.48452C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.1149+239C= MANE Select | ENSP00000260682.6:n.1149+239C= | |
| ENST00000643112.1:c.*158+239C= | ENSP00000496202.1:n.*158+239C= | |
| ENST00000260682.6:c.1149+239C= | ENSP00000260682.6:n.1149+239C= | |
| NM_000771.3:c.1149+239C= | NP_000762.2:n.1149+239C= | |
| NM_000771.4:c.1149+239C= MANE Select | NP_000762.2:n.1149+239C= |