Canonical Allele Identifier: CA182463445

Gene:

Linked Data

• dbSNP Id: rs932353182
• MyVariant Identifiers: chr8:g.98281684A>T (hg19) ; chr8:g.97269456A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269456A>T , CM000670.2:g.97269456A>T	GRCh38
NC_000008.10:g.98281684A>T , CM000670.1:g.98281684A>T	GRCh37
NC_000008.9:g.98350860A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149614T>A