Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775409A= , CM000672.2:g.94775409A= | GRCh38 |
| NC_000010.10:g.96535166A= , CM000672.1:g.96535166A= | GRCh37 |
| NC_000010.9:g.96525156A= | NCBI36 |
| NG_008384.2:g.17704A= | |
| NG_008384.3:g.17729A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.351A= MANE Select | ENSP00000360372.3:p.Gly117= | |
| ENST00000645461.1:n.1404A= | ||
| ENST00000371321.7:c.351A= | ENSP00000360372.3:p.Gly117= | |
| ENST00000464755.1:c.1114A= | ENSP00000483243.1:n.1114A= | |
| ENST00000480405.2:c.351A= | ENSP00000483847.1:p.Gly117= | |
| NM_000769.2:c.351A= | NP_000760.1:p.Gly117= | |
| NM_000769.4:c.351A= MANE Select | NP_000760.1:p.Gly117= |