Canonical Allele Identifier: CA202784133

Gene:

Linked Data

• dbSNP Id: rs966454761
• MyVariant Identifiers: chr10:g.8701139A>T (hg19) ; chr10:g.8659176A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8659176A>T , CM000672.2:g.8659176A>T	GRCh38
NC_000010.10:g.8701139A>T , CM000672.1:g.8701139A>T	GRCh37
NC_000010.9:g.8741145A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930641.1:n.172T>A
XR_001747277.1:n.141T>A