Canonical Allele Identifier: CA1886690288
Gene:

Linked Data

dbSNP Id: rs1831781516

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366799G>A , CM000672.2:g.3366799G>A GRCh38
NC_000010.10:g.3408991G>A , CM000672.1:g.3408991G>A GRCh37
NC_000010.9:g.3398991G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47943G>A