Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.96416117C= , CM000667.2:g.96416117C= | GRCh38 |
| NC_000005.9:g.95751821C= , CM000667.1:g.95751821C= | GRCh37 |
| NC_000005.8:g.95777577C= | NCBI36 |
| NG_021161.1:g.22165G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311106.8:c.625G= MANE Select | ENSP00000308024.2:p.Gly209= | |
| ENST00000311106.7:c.625G= | ENSP00000308024.2:p.Gly209= | |
| ENST00000508626.5:c.484G= | ENSP00000421600.1:p.Gly162= | |
| NM_000439.4:c.625G= | NP_000430.3:p.Gly209= | |
| NM_001177875.1:c.484G= | NP_001171346.1:p.Gly162= | |
| NR_130776.1:n.354+36465C= | ||
| NM_000439.5:c.625G= MANE Select | NP_000430.3:p.Gly209= | |
| NM_001177875.2:c.484G= | NP_001171346.1:p.Gly162= |