Canonical Allele Identifier: CA275962881

Gene:

Linked Data

• dbSNP Id: rs1005081041
• MyVariant Identifiers: chr15:g.95318637G>A (hg19) ; chr15:g.94775408G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.94775408G>A , CM000677.2:g.94775408G>A	GRCh38
NC_000015.9:g.95318637G>A , CM000677.1:g.95318637G>A	GRCh37
NC_000015.8:g.93119641G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_932644.1:n.369-9391C>T
XR_932644.2:n.369-9391C>T