Canonical Allele Identifier: CA180418665

Gene:

Linked Data

• dbSNP Id: rs762112135
• MyVariant Identifiers: chr8:g.79191046A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191046A>T , CM000670.2:g.79191046A>T	GRCh38
NC_000008.10:g.80103281A>T , CM000670.1:g.80103281A>T	GRCh37
NC_000008.9:g.80265836A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745720.1:n.105+675A>T