Canonical Allele Identifier: CA716729394

Gene:

Linked Data

• dbSNP Id: rs1484341736
• MyVariant Identifiers: chr15:g.87962752A>C (hg19) ; chr15:g.87419521A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419521A>C , CM000677.2:g.87419521A>C	GRCh38
NC_000015.9:g.87962752A>C , CM000677.1:g.87962752A>C	GRCh37
NC_000015.8:g.85763756A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.339+208T>G
XR_932585.1:n.339+208T>G
XR_001751647.1:n.616+208T>G
XR_932585.2:n.626+208T>G