Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94981669C= , CM000672.2:g.94981669C= | GRCh38 |
| NC_000010.10:g.96741426C= , CM000672.1:g.96741426C= | GRCh37 |
| NC_000010.9:g.96731416C= | NCBI36 |
| NG_008385.1:g.48012C= | |
| NG_008385.2:g.48512C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000771.4:c.1149+299C= MANE Select | NP_000762.2:n.1149+299C= |
| ENST00000260682.8:c.1149+299C= MANE Select | ENSP00000260682.6:n.1149+299C= |
| NM_000771.3:c.1149+299C= | NP_000762.2:n.1149+299C= |
| ENST00000260682.6:c.1149+299C= | ENSP00000260682.6:n.1149+299C= |
| ENST00000643112.1:c.*158+299C= | ENSP00000496202.1:n.*158+299C= |