Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781858C= , CM000672.2:g.94781858C= | GRCh38 |
| NC_000010.10:g.96541615C= , CM000672.1:g.96541615C= | GRCh37 |
| NC_000010.9:g.96531605C= | NCBI36 |
| NG_008384.2:g.24153C= | |
| NG_008384.3:g.24178C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000769.4:c.680C= MANE Select | NP_000760.1:p.Pro227= |
| ENST00000371321.9:c.680C= MANE Select | ENSP00000360372.3:p.Pro227= |
| NM_000769.2:c.680C= | NP_000760.1:p.Pro227= |
| ENST00000371321.7:c.680C= | ENSP00000360372.3:p.Pro227= |
| ENST00000464755.1:c.1443C= | ENSP00000483243.1:n.1443C= |
| ENST00000645461.1:n.1733C= |