Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.54495139C>A , CM000685.2:g.54495139C>A | GRCh38 |
| NC_000023.10:g.54521572C>A , CM000685.1:g.54521572C>A | GRCh37 |
| NC_000023.9:g.54538297C>A | NCBI36 |
| NG_008054.1:g.6028G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375135.4:c.294G>T MANE Select | ENSP00000364277.3:p.Ser98= | |
| ENST00000375135.3:c.294G>T | ENSP00000364277.3:p.Ser98= | |
| NM_004463.2:c.294G>T | NP_004454.2:p.Ser98= | |
| NM_004463.3:c.294G>T MANE Select | NP_004454.2:p.Ser98= |