Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94046951C>T , CM000663.2:g.94046951C>T | GRCh38 |
| NC_000001.10:g.94512507C>T , CM000663.1:g.94512507C>T | GRCh37 |
| NC_000001.9:g.94285095C>T | NCBI36 |
| NG_009073.1:g.79199G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370225.4:c.2886G>A MANE Select | ENSP00000359245.3:p.Leu962= | |
| ENST00000649773.1:c.2664G>A | ENSP00000496882.1:p.Leu888= | |
| ENST00000370225.3:c.2886G>A | ENSP00000359245.3:p.Leu962= | |
| ENST00000536513.5:c.-64-6862G>A | ENSP00000439707.2:n.-64-6862G>A | |
| NM_000350.2:c.2886G>A | NP_000341.2:p.Leu962= | |
| NM_000350.3:c.2886G>A MANE Select | NP_000341.2:p.Leu962= |