Canonical Allele Identifier: CA883793414

Gene:

Linked Data

• dbSNP Id: rs1417333516
• MyVariant Identifiers: chr19:g.56265666A>G (hg19) ; chr19:g.55754300A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55754300A>G , CM000681.2:g.55754300A>G	GRCh38
NC_000019.9:g.56265666A>G , CM000681.1:g.56265666A>G	GRCh37
NC_000019.8:g.60957478A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_936081.1:n.169A>G
XR_936081.2:n.228A>G