Canonical Allele Identifier: CA239906886
Gene:

Linked Data

dbSNP Id: rs12582659

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.75670748T>C , CM000674.2:g.75670748T>C GRCh38
NC_000012.11:g.76064528T>C , CM000674.1:g.76064528T>C GRCh37
NC_000012.10:g.74350795T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945107.1:n.452-6942A>G
XR_001749214.2:n.2193-6942A>G
XR_002957419.1:n.2441-6942A>G