Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94077725C>A , CM000663.2:g.94077725C>A | GRCh38 |
| NC_000001.10:g.94543281C>A , CM000663.1:g.94543281C>A | GRCh37 |
| NC_000001.9:g.94315869C>A | NCBI36 |
| NG_009073.1:g.48425G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.1519G>T MANE Select | NP_000341.2:p.Asp507Tyr |
| ENST00000370225.4:c.1519G>T MANE Select | ENSP00000359245.3:p.Asp507Tyr |
| NM_000350.2:c.1519G>T | NP_000341.2:p.Asp507Tyr |
| ENST00000370225.3:c.1519G>T | ENSP00000359245.3:p.Asp507Tyr |
| ENST00000649773.1:c.1519G>T | ENSP00000496882.1:p.Asp507Tyr |