Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046377G>C , CM000667.2:g.136046377G>C | GRCh38 |
| NC_000005.9:g.135382066G>C , CM000667.1:g.135382066G>C | GRCh37 |
| NC_000005.8:g.135409965G>C | NCBI36 |
| NG_012646.1:g.22483G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.341G>C MANE Select | ENSP00000416330.2:p.Gly114Ala | |
| ENST00000442011.6:c.341G>C | ENSP00000416330.2:p.Gly114Ala | |
| ENST00000504185.5:n.498G>C | ||
| ENST00000506699.5:n.406G>C | ||
| ENST00000507018.5:c.258G>C | ||
| ENST00000515433.1:n.633G>C | ||
| NM_000358.2:c.341G>C | NP_000349.1:p.Gly114Ala | |
| NM_000358.3:c.341G>C MANE Select | NP_000349.1:p.Gly114Ala |