Canonical Allele Identifier: CA31701797
Gene:

Linked Data

dbSNP Id: rs1007179414

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649383G>A , CM000663.2:g.168649383G>A GRCh38
NC_000001.10:g.168618621G>A , CM000663.1:g.168618621G>A GRCh37
NC_000001.9:g.166885245G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8108C>T
XR_922259.2:n.332-8108C>T