Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.22032908G>A , CM000685.2:g.22032908G>A | GRCh38 |
| NC_000023.10:g.22051026G>A , CM000685.1:g.22051026G>A | GRCh37 |
| NC_000023.9:g.21960947G>A | NCBI36 |
| NG_007563.2:g.5106G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475778.2:n.329G>A | ||
| ENST00000683214.1:n.329G>A | ||
| ENST00000684143.1:c.-98G>A | ENSP00000508264.1:n.-98G>A | |
| ENST00000379374.5:c.-98G>A MANE Select | ENSP00000368682.4:n.-98G>A | |
| ENST00000379374.4:c.-98G>A | ENSP00000368682.4:n.-98G>A | |
| NM_000444.5:c.-98G>A | NP_000435.3:n.-98G>A | |
| NM_001282754.1:c.-98G>A | NP_001269683.1:n.-98G>A | |
| XM_011545535.1:c.-98G>A | XP_011543837.1:n.-98G>A | |
| XR_001755695.1:n.582G>A | ||
| NM_000444.6:c.-98G>A MANE Select | NP_000435.3:n.-98G>A | |
| NM_001282754.2:c.-98G>A | NP_001269683.1:n.-98G>A |