Canonical Allele Identifier: CA1111858672
Gene:

Linked Data

dbSNP Id: rs10503733

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23676505G>A , CM000670.2:g.23676505G>A GRCh38
NC_000008.10:g.23534018G>A , CM000670.1:g.23534018G>A GRCh37
NC_000008.9:g.23589963G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745842.1:n.1312+7755G>A