Canonical Allele Identifier: CA275015082

Gene:

Linked Data

• dbSNP Id: rs904146183
• gnomAD v2: 15-87962591-G-A
• gnomAD v3: 15-87419360-G-A
• gnomAD v4: 15-87419360-G-A
• MyVariant Identifiers: chr15:g.87962591G>A (hg19) ; chr15:g.87419360G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419360G>A , CM000677.2:g.87419360G>A	GRCh38
NC_000015.9:g.87962591G>A , CM000677.1:g.87962591G>A	GRCh37
NC_000015.8:g.85763595G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-89C>T
XR_932585.1:n.340-89C>T
XR_001751647.1:n.617-89C>T
XR_932585.2:n.627-89C>T