Canonical Allele Identifier: CA717476259

Gene:

Linked Data

• dbSNP Id: rs1270919748
• gnomAD v3: 15-95782375-T-A
• gnomAD v4: 15-95782375-T-A
• MyVariant Identifiers: chr15:g.96325604T>A (hg19) ; chr15:g.95782375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.95782375T>A , CM000677.2:g.95782375T>A	GRCh38
NC_000015.9:g.96325604T>A , CM000677.1:g.96325604T>A	GRCh37
NC_000015.8:g.94126608T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932654.1:n.148-42814T>A