Canonical Allele Identifier: CA185200449

Gene:

Linked Data

• dbSNP Id: rs1000160364
• MyVariant Identifiers: chr8:g.123408447A>G (hg19) ; chr8:g.122396208A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122396208A>G , CM000670.2:g.122396208A>G	GRCh38
NC_000008.10:g.123408447A>G , CM000670.1:g.123408447A>G	GRCh37
NC_000008.9:g.123477628A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+2964T>C
XR_928599.3:n.152+2964T>C