Canonical Allele Identifier: CA265581603

Gene:

Linked Data

• dbSNP Id: rs373037812
• MyVariant Identifiers: chr14:g.92780919G>A (hg19) ; chr14:g.92314575G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92314575G>A , CM000676.2:g.92314575G>A	GRCh38
NC_000014.8:g.92780919G>A , CM000676.1:g.92780919G>A	GRCh37
NC_000014.7:g.91850672G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944153.1:n.132-671G>A