Canonical Allele Identifier: CA716728528

Gene:

Linked Data

• dbSNP Id: rs1245330781
• MyVariant Identifiers: chr15:g.87695419A>G (hg19) ; chr15:g.87152188A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87152188A>G , CM000677.2:g.87152188A>G	GRCh38
NC_000015.9:g.87695419A>G , CM000677.1:g.87695419A>G	GRCh37
NC_000015.8:g.85496423A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932582.1:n.167-26039A>G
XR_932582.2:n.167-26039A>G