Canonical Allele Identifier: CA182463651

Gene:

Linked Data

• dbSNP Id: rs1036771809
• MyVariant Identifiers: chr8:g.98281971T>C (hg19) ; chr8:g.97269743T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269743T>C , CM000670.2:g.97269743T>C	GRCh38
NC_000008.10:g.98281971T>C , CM000670.1:g.98281971T>C	GRCh37
NC_000008.9:g.98351147T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149327A>G