Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94949219C= , CM000672.2:g.94949219C= | GRCh38 |
| NC_000010.10:g.96708976C= , CM000672.1:g.96708976C= | GRCh37 |
| NC_000010.9:g.96698966C= | NCBI36 |
| NG_008385.1:g.15562C= | |
| NG_008385.2:g.16062C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.754C= MANE Select | ENSP00000260682.6:p.Gln252= | |
| ENST00000643112.1:c.754C= | ENSP00000496202.1:p.Gln252= | |
| ENST00000260682.6:c.754C= | ENSP00000260682.6:p.Gln252= | |
| ENST00000473496.1:n.525C= | ||
| NM_000771.3:c.754C= | NP_000762.2:p.Gln252= | |
| NM_000771.4:c.754C= MANE Select | NP_000762.2:p.Gln252= |