Canonical Allele Identifier: CA265581627

Gene:

Linked Data

• dbSNP Id: rs547086563
• gnomAD v3: 14-92314722-G-A
• gnomAD v4: 14-92314722-G-A
• MyVariant Identifiers: chr14:g.92781066G>A (hg19) ; chr14:g.92314722G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92314722G>A , CM000676.2:g.92314722G>A	GRCh38
NC_000014.8:g.92781066G>A , CM000676.1:g.92781066G>A	GRCh37
NC_000014.7:g.91850819G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944153.1:n.132-524G>A