Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.21737655C= , CM000685.2:g.21737655C= | GRCh38 |
| NC_000023.10:g.21755773C= , CM000685.1:g.21755773C= | GRCh37 |
| NC_000023.9:g.21665694C= | NCBI36 |
| NG_031916.1:g.25506G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014332.3:c.175G= MANE Select | NP_055147.1:p.Gly59= |
| ENST00000379494.4:c.175G= MANE Select | ENSP00000368808.3:p.Gly59= |
| NM_014332.2:c.175G= | NP_055147.1:p.Gly59= |
| NR_045617.1:n.406G= | |
| NR_045617.2:n.362G= | |
| ENST00000379494.3:c.175G= | ENSP00000368808.3:p.Gly59= |
| ENST00000494525.1:n.268G= | |
| ENST00000646008.1:c.175G= | ENSP00000493671.1:p.Gly59= |