Canonical Allele Identifier: CA185200460

Gene:

Linked Data

• dbSNP Id: rs890367984
• MyVariant Identifiers: chr8:g.123408519G>A (hg19) ; chr8:g.122396280G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122396280G>A , CM000670.2:g.122396280G>A	GRCh38
NC_000008.10:g.123408519G>A , CM000670.1:g.123408519G>A	GRCh37
NC_000008.9:g.123477700G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+2892C>T
XR_928599.3:n.152+2892C>T