Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40285380T>G , CM000681.2:g.40285380T>G | GRCh38 |
| NC_000019.9:g.40791287T>G , CM000681.1:g.40791287T>G | GRCh37 |
| NC_000019.8:g.45483127T>G | NCBI36 |
| NG_012038.2:g.4979A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392038.6:c.-284A>C | ENSP00000375892.2:n.-284A>C | |
| ENST00000424901.5:c.-284A>C | ENSP00000399532.2:n.-284A>C | |
| ENST00000578123.5:c.-85+68A>C | ENSP00000462022.1:n.-85+68A>C | |
| NM_001243027.2:c.-433A>C | NP_001229956.1:n.-433A>C | |
| NM_001243028.2:c.-340A>C | NP_001229957.1:n.-340A>C | |
| NM_001626.5:c.-284A>C | NP_001617.1:n.-284A>C | |
| XM_011526620.1:c.-85+68A>C | XP_011524922.1:n.-85+68A>C |