Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.42512193C>G , CM000664.2:g.42512193C>G | GRCh38 |
| NC_000002.11:g.42739333C>G , CM000664.1:g.42739333C>G | GRCh37 |
| NC_000002.10:g.42592837C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001282755.1:c.-141+16939C>G | NP_001269684.1:n.-141+16939C>G |
| NM_001282755.2:c.-141+16939C>G | NP_001269684.1:n.-141+16939C>G |
| ENST00000405592.5:c.-141+16939C>G | ENSP00000383973.1:n.-141+16939C>G |
| XM_005264459.2:c.-141+16939C>G | XP_005264516.1:n.-141+16939C>G |