Canonical Allele Identifier: CA180418736

Gene:

Linked Data

• dbSNP Id: rs1034561071
• MyVariant Identifiers: chr8:g.79191195G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191195G>T , CM000670.2:g.79191195G>T	GRCh38
NC_000008.10:g.80103430G>T , CM000670.1:g.80103430G>T	GRCh37
NC_000008.9:g.80265985G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745720.1:n.105+824G>T