Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.132785648G>T , CM000672.2:g.132785648G>T | GRCh38 |
| NC_000010.10:g.134599152G>T , CM000672.1:g.134599152G>T | GRCh37 |
| NC_000010.9:g.134449142G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_177400.3:c.301C>A MANE Select | NP_796374.2:p.Arg101Ser |
| ENST00000368592.8:c.301C>A MANE Select | ENSP00000357581.5:p.Arg101Ser |
| NM_177400.2:c.301C>A | NP_796374.1:p.Arg101Ser |
| ENST00000368592.7:c.301C>A | ENSP00000357581.5:p.Arg101Ser |
| XM_017016789.2:c.301C>A | XP_016872278.1:p.Arg101Ser |