Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23682759C>G , CM000670.2:g.23682759C>G | GRCh38 |
| NC_000008.10:g.23540272C>G , CM000670.1:g.23540272C>G | GRCh37 |
| NC_000008.9:g.23596217C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380871.5:c.131G>C MANE Select | ENSP00000370253.4:p.Gly44Ala | |
| ENST00000380871.4:c.131G>C | ENSP00000370253.4:p.Gly44Ala | |
| ENST00000523261.1:c.33+98G>C | ENSP00000429729.1:n.33+98G>C | |
| NM_001256339.1:c.33+98G>C | NP_001243268.1:n.33+98G>C | |
| NM_006167.3:c.131G>C | NP_006158.2:p.Gly44Ala | |
| NR_046072.1:n.18+145G>C | ||
| XR_001745842.1:n.1312+14009C>G | ||
| NM_006167.4:c.131G>C MANE Select | NP_006158.2:p.Gly44Ala | |
| NR_046072.2:n.35+145G>C |