Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68446785A>G , CM000663.2:g.68446785A>G | GRCh38 |
| NC_000001.10:g.68912468A>G , CM000663.1:g.68912468A>G | GRCh37 |
| NC_000001.9:g.68685056A>G | NCBI36 |
| NG_008472.1:g.8175T>C | |
| NG_008472.2:g.8175T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000329.3:c.170T>C MANE Select | NP_000320.1:p.Phe57Ser |
| ENST00000262340.6:c.170T>C MANE Select | ENSP00000262340.5:p.Phe57Ser |
| NM_000329.2:c.170T>C | NP_000320.1:p.Phe57Ser |
| ENST00000262340.5:c.170T>C | ENSP00000262340.5:p.Phe57Ser |
| XM_017002027.1:c.-32+1839T>C | XP_016857516.1:n.-32+1839T>C |