Canonical Allele Identifier: CA846669350

Gene:

Linked Data

• dbSNP Id: rs1320629815
• MyVariant Identifiers: chr8:g.123408443T>A (hg19) ; chr8:g.122396204T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122396204T>A , CM000670.2:g.122396204T>A	GRCh38
NC_000008.10:g.123408443T>A , CM000670.1:g.123408443T>A	GRCh37
NC_000008.9:g.123477624T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+2968A>T
XR_928599.3:n.152+2968A>T