Canonical Allele Identifier: CA173376542

Gene:

Linked Data

• dbSNP Id: rs1029063278
• MyVariant Identifiers: chr8:g.19987751C>T (hg19) ; chr8:g.20130240C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20130240C>T , CM000670.2:g.20130240C>T	GRCh38
NC_000008.10:g.19987751C>T , CM000670.1:g.19987751C>T	GRCh37
NC_000008.9:g.20032031C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949563.1:n.3408+321C>T
XR_949563.2:n.3400+321C>T