Canonical Allele Identifier: CA274976209

Gene:

Linked Data

• dbSNP Id: rs778313324
• gnomAD v3: 15-87152197-G-A
• gnomAD v4: 15-87152197-G-A
• MyVariant Identifiers: chr15:g.87695428G>A (hg19) ; chr15:g.87152197G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152197G>A , CM000677.2:g.87152197G>A	GRCh38
NC_000015.9:g.87695428G>A , CM000677.1:g.87695428G>A	GRCh37
NC_000015.8:g.85496432G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26030G>A
XR_932582.2:n.167-26030G>A