Canonical Allele Identifier: CA716729241

Gene:

Linked Data

• dbSNP Id: rs1400811443
• MyVariant Identifiers: chr15:g.87962579C>A (hg19) ; chr15:g.87419348C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419348C>A , CM000677.2:g.87419348C>A	GRCh38
NC_000015.9:g.87962579C>A , CM000677.1:g.87962579C>A	GRCh37
NC_000015.8:g.85763583C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-77G>T
XR_932585.1:n.340-77G>T
XR_001751647.1:n.617-77G>T
XR_932585.2:n.627-77G>T