Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.49513151G>T , CM000682.2:g.49513151G>T | GRCh38 |
| NC_000020.10:g.48129688G>T , CM000682.1:g.48129688G>T | GRCh37 |
| NC_000020.9:g.47563095G>T | NCBI36 |
| NG_007940.1:g.60020C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000961.4:c.1135C>A MANE Select | NP_000952.1:p.Arg379Ser |
| ENST00000244043.5:c.1135C>A MANE Select | ENSP00000244043.3:p.Arg379Ser |
| NM_000961.3:c.1135C>A | NP_000952.1:p.Arg379Ser |
| ENST00000244043.4:c.1135C>A | ENSP00000244043.3:p.Arg379Ser |
| ENST00000478971.1:n.956C>A |