Canonical Allele Identifier: CA716728523

Gene:

Linked Data

• dbSNP Id: rs1424798325
• gnomAD v3: 15-87152185-T-C
• gnomAD v4: 15-87152185-T-C
• MyVariant Identifiers: chr15:g.87695416T>C (hg19) ; chr15:g.87152185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152185T>C , CM000677.2:g.87152185T>C	GRCh38
NC_000015.9:g.87695416T>C , CM000677.1:g.87695416T>C	GRCh37
NC_000015.8:g.85496420T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26042T>C
XR_932582.2:n.167-26042T>C