Canonical Allele Identifier: CA721980871

Gene:

Linked Data

• dbSNP Id: rs1378705856
• gnomAD v3: 16-56610657-T-C
• gnomAD v4: 16-56610657-T-C
• MyVariant Identifiers: chr16:g.56644569T>C (hg19) ; chr16:g.56610657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56610657T>C , CM000678.2:g.56610657T>C	GRCh38
NC_000016.9:g.56644569T>C , CM000678.1:g.56644569T>C	GRCh37
NC_000016.8:g.55202070T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_933616.1:n.605+659A>G