Canonical Allele Identifier: CA709928495

Gene:

Linked Data

• dbSNP Id: rs1407339928
• MyVariant Identifiers: chr14:g.92780966G>A (hg19) ; chr14:g.92314622G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92314622G>A , CM000676.2:g.92314622G>A	GRCh38
NC_000014.8:g.92780966G>A , CM000676.1:g.92780966G>A	GRCh37
NC_000014.7:g.91850719G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944153.1:n.132-624G>A