Canonical Allele Identifier: CA202788765

Gene:

Linked Data

• dbSNP Id: rs912929526
• MyVariant Identifiers: chr10:g.8697420C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697420C>T , CM000672.2:g.8697420C>T	GRCh38
NC_000010.10:g.8739383C>T , CM000672.1:g.8739383C>T	GRCh37
NC_000010.9:g.8779389C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27619G>A