Canonical Allele Identifier: CA280619713

Gene: VKORC1

Linked Data

• dbSNP Id: rs11540137
• gnomAD v4: 16-31091003-G-T
• MyVariant Identifiers: chr16:g.31102324G>T (hg19) ; chr16:g.31091003G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091003G>T , CM000678.2:g.31091003G>T	GRCh38
NC_000016.9:g.31102324G>T , CM000678.1:g.31102324G>T	GRCh37
NC_000016.8:g.31009825G>T	NCBI36
NG_011564.1:g.8953C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.*131C>A MANE Select	ENSP00000378426.2:n.*131C>A
ENST00000300851.10:c.*234C>A	ENSP00000300851.6:n.*234C>A
ENST00000319788.11:c.*234C>A	ENSP00000326135.7:n.*234C>A
ENST00000354895.4:c.*234C>A	ENSP00000346969.4:n.*234C>A
ENST00000394975.2:c.*131C>A	ENSP00000378426.2:n.*131C>A
ENST00000420057.2:c.585C>A
ENST00000529564.1:c.283+2309C>A	ENSP00000431371.1:n.283+2309C>A
ENST00000532364.1:c.173+3554C>A	ENSP00000460316.1:n.173+3554C>A
ENST00000533518.5:c.407+89C>A
NM_001311311.1:c.*131C>A	NP_001298240.1:n.*131C>A
NM_024006.4:c.*131C>A	NP_076869.1:n.*131C>A
NM_024006.5:c.*131C>A	NP_076869.1:n.*131C>A
NM_206824.1:c.*234C>A	NP_996560.1:n.*234C>A
NM_206824.2:c.*234C>A	NP_996560.1:n.*234C>A
XM_011545944.1:c.*131C>A	XP_011544246.1:n.*131C>A
XM_011545945.1:c.*234C>A	XP_011544247.1:n.*234C>A
XR_950848.1:n.1411C>A
NM_024006.6:c.*131C>A MANE Select	NP_076869.1:n.*131C>A
NM_001311311.2:c.*131C>A	NP_001298240.1:n.*131C>A
NM_206824.3:c.*234C>A	NP_996560.1:n.*234C>A