Canonical Allele Identifier: CA275962879

Gene:

Linked Data

• dbSNP Id: rs558094253
• gnomAD v2: 15-95318633-T-A
• gnomAD v3: 15-94775404-T-A
• gnomAD v4: 15-94775404-T-A
• MyVariant Identifiers: chr15:g.95318633T>A (hg19) ; chr15:g.94775404T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.94775404T>A , CM000677.2:g.94775404T>A	GRCh38
NC_000015.9:g.95318633T>A , CM000677.1:g.95318633T>A	GRCh37
NC_000015.8:g.93119637T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_932644.1:n.369-9387A>T
XR_932644.2:n.369-9387A>T