Canonical Allele Identifier:
CA2752787479
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.155870769C>A , CM000664.2:g.155870769C>A | GRCh38 |
| NC_000002.11:g.156727281C>A , CM000664.1:g.156727281C>A | GRCh37 |
| NC_000002.10:g.156435527C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923501.1:n.320-3582G>T | ||
| XR_001739749.1:n.331-29785G>T | ||
| XR_001739750.1:n.331-29785G>T | ||
| XR_001739751.1:n.331-29785G>T | ||
| XR_923501.2:n.331-3582G>T |