Canonical Allele Identifier: CA883793437

Gene:

Linked Data

• dbSNP Id: rs1286220049
• gnomAD v3: 19-55754342-C-A
• gnomAD v4: 19-55754342-C-A
• MyVariant Identifiers: chr19:g.56265708C>A (hg19) ; chr19:g.55754342C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55754342C>A , CM000681.2:g.55754342C>A	GRCh38
NC_000019.9:g.56265708C>A , CM000681.1:g.56265708C>A	GRCh37
NC_000019.8:g.60957520C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_936081.1:n.211C>A
XR_936081.2:n.270C>A