Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50192897C= , CM000685.2:g.50192897C= | GRCh38 |
| NC_000023.10:g.49957548C= , CM000685.1:g.49957548C= | GRCh37 |
| NC_000023.9:g.49844288C= | NCBI36 |
| NG_012552.1:g.13117G= | |
| NG_012552.2:g.13117G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358526.7:c.1816G= MANE Select | ENSP00000351327.2:p.Ala606= | |
| ENST00000358526.6:c.1816G= | ENSP00000351327.2:p.Ala606= | |
| ENST00000376064.7:c.1789G= | ENSP00000365232.3:p.Ala597= | |
| ENST00000481402.5:n.1928G= | ||
| NM_003886.2:c.1816G= | NP_003877.2:p.Ala606= | |
| NM_139289.1:c.1789G= | NP_647450.1:p.Ala597= | |
| NM_003886.3:c.1816G= MANE Select | NP_003877.2:p.Ala606= | |
| NM_139289.2:c.1789G= | NP_647450.1:p.Ala597= |