Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23222659A>G , CM000670.2:g.23222659A>G | GRCh38 |
| NC_000008.10:g.23080172A>G , CM000670.1:g.23080172A>G | GRCh37 |
| NC_000008.9:g.23136117A>G | NCBI36 |
| NG_032107.1:g.7509T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000221132.8:c.306+2097T>C MANE Select | ENSP00000221132.3:n.306+2097T>C | |
| ENST00000221132.7:c.306+2097T>C | ENSP00000221132.3:n.306+2097T>C | |
| ENST00000524158.5:c.-301+1774T>C | ENSP00000428884.1:n.-301+1774T>C | |
| ENST00000613472.1:c.31+2372T>C | ENSP00000480778.1:n.31+2372T>C | |
| NM_003844.3:c.306+2097T>C | NP_003835.3:n.306+2097T>C | |
| NM_003844.4:c.306+2097T>C MANE Select | NP_003835.3:n.306+2097T>C |