Canonical Allele Identifier: CA275015081

Gene:

Linked Data

• dbSNP Id: rs1042776257
• MyVariant Identifiers: chr15:g.87962582A>G (hg19) ; chr15:g.87419351A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419351A>G , CM000677.2:g.87419351A>G	GRCh38
NC_000015.9:g.87962582A>G , CM000677.1:g.87962582A>G	GRCh37
NC_000015.8:g.85763586A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-80T>C
XR_932585.1:n.340-80T>C
XR_001751647.1:n.617-80T>C
XR_932585.2:n.627-80T>C