Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30737326G>A , CM000678.2:g.30737326G>A | GRCh38 |
| NC_000016.9:g.30748647G>A , CM000678.1:g.30748647G>A | GRCh37 |
| NC_000016.8:g.30656148G>A | NCBI36 |
| NG_032135.1:g.43186G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006662.3:c.7286G>A MANE Select | NP_006653.2:p.Cys2429Tyr |
| ENST00000262518.9:c.7286G>A MANE Select | ENSP00000262518.4:p.Cys2429Tyr |
| NM_006662.2:c.7286G>A | NP_006653.2:p.Cys2429Tyr |
| ENST00000262518.8:c.7286G>A | ENSP00000262518.4:p.Cys2429Tyr |
| ENST00000380361.7:c.6755G>A | ENSP00000369719.3:p.Cys2252Tyr |
| ENST00000395059.6:c.6509G>A | ENSP00000378499.3:p.Cys2170Tyr |
| ENST00000411466.7:c.7286G>A | ENSP00000405186.3:p.Cys2429Tyr |
| ENST00000704023.1:c.1566G>A | |
| ENST00000706321.1:c.7286G>A | ENSP00000516346.1:p.Cys2429Tyr |