Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19116739C= , CM000669.2:g.19116739C= | GRCh38 |
| NC_000007.13:g.19156362C= , CM000669.1:g.19156362C= | GRCh37 |
| NC_000007.12:g.19122887C= | NCBI36 |
| NG_008114.1:g.5934G= | |
| NG_008114.2:g.5934G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.583G= MANE Select | ENSP00000242261.5:p.Ala195= | |
| ENST00000242261.5:c.583G= | ENSP00000242261.5:p.Ala195= | |
| ENST00000354571.5:c.380G= | ||
| ENST00000443687.5:c.186G= | ||
| NM_000474.3:c.583G= | NP_000465.1:p.Ala195= | |
| XM_011515496.1:c.583G= | XP_011513798.1:p.Ala195= | |
| NR_149001.1:n.934G= | ||
| NM_000474.4:c.583G= MANE Select | NP_000465.1:p.Ala195= | |
| NR_149001.2:n.898G= |