Canonical Allele Identifier: CA716729226

Gene:

Linked Data

• dbSNP Id: rs376925797
• gnomAD v3: 15-87419308-G-A
• gnomAD v4: 15-87419308-G-A
• MyVariant Identifiers: chr15:g.87962539G>A (hg19) ; chr15:g.87419308G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419308G>A , CM000677.2:g.87419308G>A	GRCh38
NC_000015.9:g.87962539G>A , CM000677.1:g.87962539G>A	GRCh37
NC_000015.8:g.85763543G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-37C>T
XR_932585.1:n.340-37C>T
XR_001751647.1:n.617-37C>T
XR_932585.2:n.627-37C>T