Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23431665C>A , CM000676.2:g.23431665C>A | GRCh38 |
| NC_000014.8:g.23900874C>A , CM000676.1:g.23900874C>A | GRCh37 |
| NC_000014.7:g.22970714C>A | NCBI36 |
| NG_007884.1:g.8997G>T , LRG_384:g.8997G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.652G>T MANE Select | ENSP00000347507.3:p.Asp218Tyr | |
| ENST00000355349.3:c.652G>T | ENSP00000347507.3:p.Asp218Tyr | |
| NM_000257.3:c.652G>T | NP_000248.2:p.Asp218Tyr | |
| XR_245686.3:n.758G>T | ||
| XM_017021340.1:c.652G>T | XP_016876829.1:p.Asp218Tyr | |
| NM_000257.4:c.652G>T MANE Select | NP_000248.2:p.Asp218Tyr |