Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48859097T>A , CM000665.2:g.48859097T>A | GRCh38 |
| NC_000003.11:g.48896530T>A , CM000665.1:g.48896530T>A | GRCh37 |
| NC_000003.10:g.48871534T>A | NCBI36 |
| NG_008171.1:g.44800A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319017.5:c.713A>T MANE Select | ENSP00000326305.4:p.Gln238Leu | |
| ENST00000319017.4:c.713A>T | ENSP00000326305.4:p.Gln238Leu | |
| ENST00000430379.5:c.494A>T | ENSP00000388986.1:p.Gln165Leu | |
| ENST00000440964.1:c.*543A>T | ENSP00000388563.1:n.*543A>T | |
| NM_000387.5:c.713A>T | NP_000378.1:p.Gln238Leu | |
| XM_006713327.1:c.536-1325A>T | XP_006713390.1:n.536-1325A>T | |
| NM_000387.6:c.713A>T MANE Select | NP_000378.1:p.Gln238Leu |