Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19116905G= , CM000669.2:g.19116905G= | GRCh38 |
| NC_000007.13:g.19156528G= , CM000669.1:g.19156528G= | GRCh37 |
| NC_000007.12:g.19123053G= | NCBI36 |
| NG_008114.1:g.5768C= | |
| NG_008114.2:g.5768C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.417C= MANE Select | ENSP00000242261.5:p.Pro139= | |
| ENST00000242261.5:c.417C= | ENSP00000242261.5:p.Pro139= | |
| ENST00000354571.5:c.214C= | ||
| ENST00000443687.5:c.20C= | ||
| NM_000474.3:c.417C= | NP_000465.1:p.Pro139= | |
| XM_011515496.1:c.417C= | XP_011513798.1:p.Pro139= | |
| NR_149001.1:n.768C= | ||
| NM_000474.4:c.417C= MANE Select | NP_000465.1:p.Pro139= | |
| NR_149001.2:n.732C= |