Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135952873T>C , CM000667.2:g.135952873T>C | GRCh38 |
| NC_000005.9:g.135288562T>C , CM000667.1:g.135288562T>C | GRCh37 |
| NC_000005.8:g.135316461T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274507.6:c.141A>G MANE Select | ENSP00000274507.1:p.Gln47= | |
| ENST00000274507.5:c.141A>G | ENSP00000274507.1:p.Gln47= | |
| ENST00000471827.1:n.244A>G | ||
| ENST00000512872.1:c.-76A>G | ENSP00000427012.1:n.-76A>G | |
| ENST00000514447.2:c.141A>G | ENSP00000421123.2:p.Gln47= | |
| ENST00000522943.5:c.141A>G | ENSP00000429618.1:p.Gln47= | |
| NM_002302.2:c.141A>G | NP_002293.2:p.Gln47= | |
| NM_002302.3:c.141A>G MANE Select | NP_002293.2:p.Gln47= |