Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31372218T>C , CM000664.2:g.31372218T>C | GRCh38 |
| NC_000002.11:g.31595084T>C , CM000664.1:g.31595084T>C | GRCh37 |
| NC_000002.10:g.31448588T>C | NCBI36 |
| NG_008871.1:g.47528A>G | |
| NG_008871.2:g.47528A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000379.4:c.1856+10A>G MANE Select | NP_000370.2:n.1856+10A>G |
| ENST00000379416.4:c.1856+10A>G MANE Select | ENSP00000368727.3:n.1856+10A>G |
| NM_000379.3:c.1856+10A>G | NP_000370.2:n.1856+10A>G |
| ENST00000379416.3:c.1856+10A>G | ENSP00000368727.3:n.1856+10A>G |
| XM_011533095.1:c.1853+10A>G | XP_011531397.1:n.1853+10A>G |
| XM_011533095.2:c.1853+10A>G | XP_011531397.1:n.1853+10A>G |
| XM_011533096.1:c.1856+10A>G | XP_011531398.1:n.1856+10A>G |
| XM_011533096.2:c.1856+10A>G | XP_011531398.1:n.1856+10A>G |