Canonical Allele Identifier: CA716729310
Gene:

Linked Data

dbSNP Id: rs1262876968
MyVariant Identifiers: chr15:g.87962677C>T (hg19) chr15:g.87419446C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419446C>T , CM000677.2:g.87419446C>T GRCh38
NC_000015.9:g.87962677C>T , CM000677.1:g.87962677C>T GRCh37
NC_000015.8:g.85763681C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-175G>A
XR_932585.1:n.340-175G>A
XR_001751647.1:n.617-175G>A
XR_932585.2:n.627-175G>A
Search 100 bp 5'
Search 100 bp 3'