Canonical Allele Identifier: CA182463538

Gene:

Linked Data

• dbSNP Id: rs376619159
• MyVariant Identifiers: chr8:g.98281807A>C (hg19) ; chr8:g.97269579A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269579A>C , CM000670.2:g.97269579A>C	GRCh38
NC_000008.10:g.98281807A>C , CM000670.1:g.98281807A>C	GRCh37
NC_000008.9:g.98350983A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125390.1:n.471+149491T>G