Canonical Allele Identifier: CA716729347

Gene:

Linked Data

• dbSNP Id: rs1165750577
• MyVariant Identifiers: chr15:g.87962727G>A (hg19) ; chr15:g.87419496G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419496G>A , CM000677.2:g.87419496G>A	GRCh38
NC_000015.9:g.87962727G>A , CM000677.1:g.87962727G>A	GRCh37
NC_000015.8:g.85763731G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_932584.1:n.340-225C>T
XR_932585.1:n.340-225C>T
XR_001751647.1:n.617-225C>T
XR_932585.2:n.627-225C>T