Canonical Allele Identifier: CA276104128

Gene:

Linked Data

• dbSNP Id: rs958864237
• gnomAD v3: 15-95782451-G-A
• gnomAD v4: 15-95782451-G-A
• MyVariant Identifiers: chr15:g.96325680G>A (hg19) ; chr15:g.95782451G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.95782451G>A , CM000677.2:g.95782451G>A	GRCh38
NC_000015.9:g.96325680G>A , CM000677.1:g.96325680G>A	GRCh37
NC_000015.8:g.94126684G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932654.1:n.148-42738G>A