Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94849995C= , CM000672.2:g.94849995C= | GRCh38 |
| NC_000010.10:g.96609752C= , CM000672.1:g.96609752C= | GRCh37 |
| NC_000010.9:g.96599742C= | NCBI36 |
| NG_008384.2:g.92290C= | |
| NG_008384.3:g.92315C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000769.4:c.1228C= MANE Select | NP_000760.1:p.Arg410= |
| ENST00000371321.9:c.1228C= MANE Select | ENSP00000360372.3:p.Arg410= |
| NM_000769.2:c.1228C= | NP_000760.1:p.Arg410= |
| ENST00000371321.7:c.1228C= | ENSP00000360372.3:p.Arg410= |
| ENST00000464755.1:c.1991C= | ENSP00000483243.1:n.1991C= |
| ENST00000645461.1:n.2139C= |