Canonical Allele Identifier: CA725798589

Gene:

Linked Data

• dbSNP Id: rs531499985
• MyVariant Identifiers: chr16:g.9343582A>T (hg19) ; chr16:g.9249725A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249725A>T , CM000678.2:g.9249725A>T	GRCh38
NC_000016.9:g.9343582A>T , CM000678.1:g.9343582A>T	GRCh37
NC_000016.8:g.9251083A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64992A>T