Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022729G= , CM000663.2:g.17022729G= | GRCh38 |
| NC_000001.10:g.17349224G= , CM000663.1:g.17349224G= | GRCh37 |
| NC_000001.9:g.17221811G= | NCBI36 |
| NG_012340.1:g.36442C= , LRG_316:g.36442C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.473C= | ENSP00000481376.2:p.Ala158= | |
| ENST00000491274.6:c.602C= | ENSP00000480482.2:p.Ala201= | |
| ENST00000375499.8:c.644C= MANE Select | ENSP00000364649.3:p.Ala215= | |
| ENST00000375499.7:c.644C= | ENSP00000364649.3:p.Ala215= | |
| ENST00000475049.5:n.69C= | ||
| ENST00000485092.5:n.308C= | ||
| ENST00000485515.5:n.578C= | ||
| NM_003000.2:c.644C= , LRG_316t1:c.644C= | NP_002991.2:p.Ala215= | |
| NM_003000.3:c.644C= MANE Select | NP_002991.2:p.Ala215= |