Canonical Allele Identifier: CA180418745

Gene:

Linked Data

• dbSNP Id: rs1006113022
• MyVariant Identifiers: chr8:g.80103435G>A (hg19) ; chr8:g.79191200G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191200G>A , CM000670.2:g.79191200G>A	GRCh38
NC_000008.10:g.80103435G>A , CM000670.1:g.80103435G>A	GRCh37
NC_000008.9:g.80265990G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745720.1:n.105+829G>A