Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150860770T>A , CM000667.2:g.150860770T>A | GRCh38 |
| NC_000005.9:g.150240332T>A , CM000667.1:g.150240332T>A | GRCh37 |
| NC_000005.8:g.150220525T>A | NCBI36 |
| NG_027809.2:g.19248T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000520549.1:c.158+12116T>A | ||
| XM_011537641.1:c.531+12116T>A | XP_011535943.1:n.531+12116T>A | |
| NM_001346557.1:c.531+12116T>A | NP_001333486.1:n.531+12116T>A | |
| NM_001346557.2:c.531+12116T>A | NP_001333486.1:n.531+12116T>A | |
| NR_170598.1:n.1646+12116T>A |