Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58273659T= , CM000679.2:g.58273659T= | GRCh38 |
| NC_000017.10:g.56351020T= , CM000679.1:g.56351020T= | GRCh37 |
| NC_000017.9:g.53706019T= | NCBI36 |
| NG_009629.1:g.12277A= , LRG_84:g.12277A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000578493.2:n.709A= | ||
| ENST00000699291.1:c.501A= | ENSP00000514272.1:p.Leu167= | |
| ENST00000699292.1:n.416A= | ||
| ENST00000225275.4:c.1376A= MANE Select | ENSP00000225275.3:p.Tyr459= | |
| ENST00000225275.3:c.1376A= | ENSP00000225275.3:p.Tyr459= | |
| NM_000250.1:c.1376A= , LRG_84t1:c.1376A= | NP_000241.1:p.Tyr459= | |
| XM_011524821.1:c.1562A= | XP_011523123.1:p.Tyr521= | |
| XM_011524822.1:c.1091A= | XP_011523124.1:p.Tyr364= | |
| XM_011524823.1:c.1401A= | XP_011523125.1:p.Leu467= | |
| NM_000250.2:c.1376A= MANE Select | NP_000241.1:p.Tyr459= |