Canonical Allele Identifier: CA856574001

Gene:

Linked Data

• dbSNP Id: rs1487528636
• MyVariant Identifiers: chr8:g.89993420A>T (hg19) ; chr8:g.88981191A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88981191A>T , CM000670.2:g.88981191A>T	GRCh38
NC_000008.10:g.89993420A>T , CM000670.1:g.89993420A>T	GRCh37
NC_000008.9:g.90062536A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956667.1:n.179-99130T>A