Canonical Allele Identifier: CA275015079

Gene:

Linked Data

• dbSNP Id: rs1028737358
• gnomAD v3: 15-87419331-T-C
• gnomAD v4: 15-87419331-T-C
• MyVariant Identifiers: chr15:g.87962562T>C (hg19) ; chr15:g.87419331T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419331T>C , CM000677.2:g.87419331T>C	GRCh38
NC_000015.9:g.87962562T>C , CM000677.1:g.87962562T>C	GRCh37
NC_000015.8:g.85763566T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-60A>G
XR_932585.1:n.340-60A>G
XR_001751647.1:n.617-60A>G
XR_932585.2:n.627-60A>G