Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94079324T>A , CM000663.2:g.94079324T>A | GRCh38 |
| NC_000001.10:g.94544880T>A , CM000663.1:g.94544880T>A | GRCh37 |
| NC_000001.9:g.94317468T>A | NCBI36 |
| NG_009073.1:g.46826A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.1237A>T MANE Select | NP_000341.2:p.Asn413Tyr |
| ENST00000370225.4:c.1237A>T MANE Select | ENSP00000359245.3:p.Asn413Tyr |
| NM_000350.2:c.1237A>T | NP_000341.2:p.Asn413Tyr |
| ENST00000370225.3:c.1237A>T | ENSP00000359245.3:p.Asn413Tyr |
| ENST00000649773.1:c.1237A>T | ENSP00000496882.1:p.Asn413Tyr |