Canonical Allele Identifier: CA716728542

Gene:

Linked Data

• dbSNP Id: rs1340860193
• gnomAD v3: 15-87152201-A-G
• gnomAD v4: 15-87152201-A-G
• MyVariant Identifiers: chr15:g.87695432A>G (hg19) ; chr15:g.87152201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152201A>G , CM000677.2:g.87152201A>G	GRCh38
NC_000015.9:g.87695432A>G , CM000677.1:g.87695432A>G	GRCh37
NC_000015.8:g.85496436A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26026A>G
XR_932582.2:n.167-26026A>G