Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19953386G= , CM000670.2:g.19953386G= | GRCh38 |
| NC_000008.10:g.19810897G= , CM000670.1:g.19810897G= | GRCh37 |
| NC_000008.9:g.19855177G= | NCBI36 |
| NG_008855.1:g.19316G= | |
| NG_008855.2:g.56670G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.506G= MANE Select | ENSP00000497642.1:p.Gly169= | |
| ENST00000311322.8:c.506G= | ENSP00000309757.6:p.Gly169= | |
| ENST00000520959.5:c.278G= | ENSP00000428496.1:p.Gly93= | |
| NM_000237.2:c.506G= | NP_000228.1:p.Gly169= | |
| NM_000237.3:c.506G= MANE Select | NP_000228.1:p.Gly169= |