Canonical Allele Identifier: CA716728475

Gene:

Linked Data

• dbSNP Id: rs939379252
• MyVariant Identifiers: chr15:g.87695390C>T (hg19) ; chr15:g.87152159C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152159C>T , CM000677.2:g.87152159C>T	GRCh38
NC_000015.9:g.87695390C>T , CM000677.1:g.87695390C>T	GRCh37
NC_000015.8:g.85496394C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26068C>T
XR_932582.2:n.167-26068C>T