Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39666005G= , CM000679.2:g.39666005G= | GRCh38 |
| NC_000017.10:g.37822258G= , CM000679.1:g.37822258G= | GRCh37 |
| NC_000017.9:g.35075784G= | NCBI36 |
| NG_008892.1:g.5660G= , LRG_210:g.5660G= | |
| NG_042278.1:g.3025G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.400G= MANE Select | ENSP00000312624.2:p.Ala134= | |
| ENST00000309889.2:c.400G= | ENSP00000312624.2:p.Ala134= | |
| ENST00000578283.1:c.328G= | ENSP00000462787.1:p.Ala110= | |
| NM_003673.3:c.400G= , LRG_210t1:c.400G= | NP_003664.1:p.Ala134= | |
| NM_003673.4:c.400G= MANE Select | NP_003664.1:p.Ala134= |