Canonical Allele Identifier: CA847118780

Gene:

Linked Data

• dbSNP Id: rs1210581556
• MyVariant Identifiers: chr8:g.128024871T>A (hg19) ; chr8:g.127012626T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127012626T>A , CM000670.2:g.127012626T>A	GRCh38
NC_000008.10:g.128024871T>A , CM000670.1:g.128024871T>A	GRCh37
NC_000008.9:g.128094053T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746076.2:n.1364+6008T>A