Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.23646320C>A , CM000677.2:g.23646320C>A | GRCh38 |
| NC_000015.9:g.23891467C>A , CM000677.1:g.23891467C>A | GRCh37 |
| NC_000015.8:g.21442560C>A | NCBI36 |
| NG_016776.1:g.6527G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019066.5:c.1423G>T MANE Select | NP_061939.3:p.Ala475Ser |
| ENST00000650528.1:c.1423G>T MANE Select | ENSP00000497810.1:p.Ala475Ser |
| NM_019066.4:c.1423G>T | NP_061939.3:p.Ala475Ser |
| ENST00000532292.2:c.1423G>T | ENSP00000433433.2:p.Ala475Ser |