Canonical Allele Identifier: CA2710203891
Gene:

Linked Data

dbSNP Id: rs2113056361

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354513A>G , CM000667.2:g.152354513A>G GRCh38
NC_000005.9:g.151734074A>G , CM000667.1:g.151734074A>G GRCh37
NC_000005.8:g.151714267A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944433.1:n.196+16650A>G
XR_944433.2:n.197+16650A>G