Canonical Allele Identifier: CA274976210

Gene:

Linked Data

• dbSNP Id: rs1010959743
• gnomAD v2: 15-87695438-G-A
• MyVariant Identifiers: chr15:g.87695438G>A (hg19) ; chr15:g.87152207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152207G>A , CM000677.2:g.87152207G>A	GRCh38
NC_000015.9:g.87695438G>A , CM000677.1:g.87695438G>A	GRCh37
NC_000015.8:g.85496442G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26020G>A
XR_932582.2:n.167-26020G>A