Canonical Allele Identifier: CA931883591
Gene:

Linked Data

dbSNP Id: rs2064898807

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750657T>C , CM000672.2:g.101750657T>C GRCh38
NC_000010.10:g.103510414T>C , CM000672.1:g.103510414T>C GRCh37
NC_000010.9:g.103500404T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6440A>G
XR_946255.2:n.217-6440A>G