Canonical Allele Identifier: CA11826504
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10517086

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083889G>A , CM000666.2:g.26083889G>A GRCh38
NC_000004.11:g.26085511G>A , CM000666.1:g.26085511G>A GRCh37
NC_000004.10:g.25694609G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3299G>A
XR_925506.3:n.1408+3299G>A