Canonical Allele Identifier: CA717476256

Gene:

Linked Data

• dbSNP Id: rs1467829405
• gnomAD v3: 15-95782373-A-G
• gnomAD v4: 15-95782373-A-G
• MyVariant Identifiers: chr15:g.96325602A>G (hg19) ; chr15:g.95782373A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.95782373A>G , CM000677.2:g.95782373A>G	GRCh38
NC_000015.9:g.96325602A>G , CM000677.1:g.96325602A>G	GRCh37
NC_000015.8:g.94126606A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932654.1:n.148-42816A>G