Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117065C= , CM000669.2:g.19117065C= | GRCh38 |
| NC_000007.13:g.19156688C= , CM000669.1:g.19156688C= | GRCh37 |
| NC_000007.12:g.19123213C= | NCBI36 |
| NG_008114.1:g.5608G= | |
| NG_008114.2:g.5608G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.257G= MANE Select | ENSP00000242261.5:p.Gly86= | |
| ENST00000242261.5:c.257G= | ENSP00000242261.5:p.Gly86= | |
| ENST00000354571.5:c.54G= | ||
| NM_000474.3:c.257G= | NP_000465.1:p.Gly86= | |
| XM_011515496.1:c.257G= | XP_011513798.1:p.Gly86= | |
| NR_149001.1:n.608G= | ||
| NM_000474.4:c.257G= MANE Select | NP_000465.1:p.Gly86= | |
| NR_149001.2:n.572G= |