Canonical Allele Identifier: CA275015074

Gene:

Linked Data

• dbSNP Id: rs575855468
• gnomAD v3: 15-87419301-G-A
• MyVariant Identifiers: chr15:g.87962532G>A (hg19) ; chr15:g.87419301G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419301G>A , CM000677.2:g.87419301G>A	GRCh38
NC_000015.9:g.87962532G>A , CM000677.1:g.87962532G>A	GRCh37
NC_000015.8:g.85763536G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-30C>T
XR_932585.1:n.340-30C>T
XR_001751647.1:n.617-30C>T
XR_932585.2:n.627-30C>T