Canonical Allele Identifier: CA205143417
Gene:

Linked Data

dbSNP Id: rs886689702

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075671A>G , CM000672.2:g.29075671A>G GRCh38
NC_000010.10:g.29364600A>G , CM000672.1:g.29364600A>G GRCh37
NC_000010.9:g.29404606A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3821A>G