Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.165425645T>A , CM000663.2:g.165425645T>A | GRCh38 |
| NC_000001.10:g.165394882T>A , CM000663.1:g.165394882T>A | GRCh37 |
| NC_000001.9:g.163661506T>A | NCBI36 |
| NG_029517.1:g.24711A>T | |
| NG_029517.2:g.24711A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359842.10:c.297+3074A>T MANE Select | ENSP00000352900.5:n.297+3074A>T | |
| ENST00000359842.9:c.297+3074A>T | ENSP00000352900.5:n.297+3074A>T | |
| ENST00000619224.1:c.-130-837A>T | ENSP00000482458.1:n.-130-837A>T | |
| NM_001256570.1:c.-130-837A>T | NP_001243499.1:n.-130-837A>T | |
| NM_006917.4:c.297+3074A>T | NP_008848.1:n.297+3074A>T | |
| NM_006917.5:c.297+3074A>T MANE Select | NP_008848.1:n.297+3074A>T | |
| NM_001256570.2:c.-130-837A>T | NP_001243499.1:n.-130-837A>T |