Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31337627G>C , CM000664.2:g.31337627G>C | GRCh38 |
| NC_000002.11:g.31560493G>C , CM000664.1:g.31560493G>C | GRCh37 |
| NC_000002.10:g.31413997G>C | NCBI36 |
| NG_008871.1:g.82119C>G | |
| NG_008871.2:g.82119C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379416.4:c.3951+14C>G MANE Select | ENSP00000368727.3:n.3951+14C>G | |
| ENST00000379416.3:c.3951+14C>G | ENSP00000368727.3:n.3951+14C>G | |
| NM_000379.3:c.3951+14C>G | NP_000370.2:n.3951+14C>G | |
| XM_011533095.1:c.3948+14C>G | XP_011531397.1:n.3948+14C>G | |
| XM_011533095.2:c.3948+14C>G | XP_011531397.1:n.3948+14C>G | |
| NM_000379.4:c.3951+14C>G MANE Select | NP_000370.2:n.3951+14C>G |