Canonical Allele Identifier: CA857362208
Gene:

Linked Data

dbSNP Id: rs1416323540

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269659G>A , CM000670.2:g.97269659G>A GRCh38
NC_000008.10:g.98281887G>A , CM000670.1:g.98281887G>A GRCh37
NC_000008.9:g.98351063G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149411C>T