Canonical Allele Identifier: CA185200368

Gene:

Linked Data

• dbSNP Id: rs910740118
• MyVariant Identifiers: chr8:g.123407894C>T (hg19) ; chr8:g.122395655C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122395655C>T , CM000670.2:g.122395655C>T	GRCh38
NC_000008.10:g.123407894C>T , CM000670.1:g.123407894C>T	GRCh37
NC_000008.9:g.123477075C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+3517G>A
XR_928599.3:n.152+3517G>A