Canonical Allele Identifier: CA1605276927
Gene:

Linked Data

dbSNP Id: rs1762570224

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465999G>A , CM000668.2:g.465999G>A GRCh38
NC_000006.11:g.465999G>A , CM000668.1:g.465999G>A GRCh37
NC_000006.10:g.410999G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12274G>A
XR_926365.1:n.2548+12274G>A
XR_001743914.1:n.482-9209G>A