Canonical Allele Identifier: CA265581605

Gene:

Linked Data

• dbSNP Id: rs17783558
• gnomAD v2: 14-92780920-G-C
• gnomAD v3: 14-92314576-G-C
• gnomAD v4: 14-92314576-G-C
• MyVariant Identifiers: chr14:g.92780920G>C (hg19) ; chr14:g.92314576G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92314576G>C , CM000676.2:g.92314576G>C	GRCh38
NC_000014.8:g.92780920G>C , CM000676.1:g.92780920G>C	GRCh37
NC_000014.7:g.91850673G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944153.1:n.132-670G>C