Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117030C= , CM000669.2:g.19117030C= | GRCh38 |
| NC_000007.13:g.19156653C= , CM000669.1:g.19156653C= | GRCh37 |
| NC_000007.12:g.19123178C= | NCBI36 |
| NG_008114.1:g.5643G= | |
| NG_008114.2:g.5643G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.292G= MANE Select | ENSP00000242261.5:p.Gly98= | |
| ENST00000242261.5:c.292G= | ENSP00000242261.5:p.Gly98= | |
| ENST00000354571.5:c.89G= | ||
| NM_000474.3:c.292G= | NP_000465.1:p.Gly98= | |
| XM_011515496.1:c.292G= | XP_011513798.1:p.Gly98= | |
| NR_149001.1:n.643G= | ||
| NM_000474.4:c.292G= MANE Select | NP_000465.1:p.Gly98= | |
| NR_149001.2:n.607G= |