Canonical Allele Identifier: CA210587

Gene: VKORC1

Linked Data

• ClinVar Variation Id: 60671
• ClinVar RCV Id: RCV000054486
• dbSNP Id: rs397509427
• MyVariant Identifiers: chr16:g.31107637_31107638insC (hg19) ; chr16:g.31096316_31096317insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31096319dup , CM000678.2:g.31096319dup	GRCh38
NC_000016.9:g.31107640dup , CM000678.1:g.31107640dup	GRCh37
NC_000016.8:g.31015141dup	NCBI36
NG_011564.1:g.3639dup

Transcript Alleles

HGVS	Amino-acid change
XR_950848.1:n.16+5dup