Canonical Allele Identifier: CA31701814
Gene:

Linked Data

dbSNP Id: rs984326513

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649432C>A , CM000663.2:g.168649432C>A GRCh38
NC_000001.10:g.168618670C>A , CM000663.1:g.168618670C>A GRCh37
NC_000001.9:g.166885294C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8157G>T
XR_922259.2:n.332-8157G>T