Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.21743773C= , CM000685.2:g.21743773C= | GRCh38 |
| NC_000023.10:g.21761891C= , CM000685.1:g.21761891C= | GRCh37 |
| NC_000023.9:g.21671812C= | NCBI36 |
| NG_031916.1:g.19388G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379494.4:c.109G= MANE Select | ENSP00000368808.3:p.Glu37= | |
| ENST00000646008.1:c.109G= | ENSP00000493671.1:p.Glu37= | |
| ENST00000379494.3:c.109G= | ENSP00000368808.3:p.Glu37= | |
| ENST00000494525.1:n.202G= | ||
| NM_014332.2:c.109G= | NP_055147.1:p.Glu37= | |
| NR_045617.1:n.340G= | ||
| NM_014332.3:c.109G= MANE Select | NP_055147.1:p.Glu37= | |
| NR_045617.2:n.296G= |