Canonical Allele Identifier: CA709928467

Gene:

Linked Data

• dbSNP Id: rs1342462073
• gnomAD v3: 14-92314595-C-G
• gnomAD v4: 14-92314595-C-G
• MyVariant Identifiers: chr14:g.92780939C>G (hg19) ; chr14:g.92314595C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92314595C>G , CM000676.2:g.92314595C>G	GRCh38
NC_000014.8:g.92780939C>G , CM000676.1:g.92780939C>G	GRCh37
NC_000014.7:g.91850692C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944153.1:n.132-651C>G