Canonical Allele Identifier: CA846669077

Gene:

Linked Data

• dbSNP Id: rs1191567193
• MyVariant Identifiers: chr8:g.123407924C>T (hg19) ; chr8:g.122395685C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122395685C>T , CM000670.2:g.122395685C>T	GRCh38
NC_000008.10:g.123407924C>T , CM000670.1:g.123407924C>T	GRCh37
NC_000008.9:g.123477105C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+3487G>A
XR_928599.3:n.152+3487G>A