Canonical Allele Identifier: CA719893508

Gene: VKORC1

Linked Data

• dbSNP Id: rs1487878860
• gnomAD v3: 16-31093953-C-T
• gnomAD v4: 16-31093953-C-T
• MyVariant Identifiers: chr16:g.31105274C>T (hg19) ; chr16:g.31093953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093953C>T , CM000678.2:g.31093953C>T	GRCh38
NC_000016.9:g.31105274C>T , CM000678.1:g.31105274C>T	GRCh37
NC_000016.8:g.31012775C>T	NCBI36
NG_011564.1:g.6003G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.174-532G>A MANE Select	ENSP00000378426.2:n.174-532G>A
ENST00000300851.10:c.174-471G>A	ENSP00000300851.6:n.174-471G>A
ENST00000319788.11:c.174-532G>A	ENSP00000326135.7:n.174-532G>A
ENST00000354895.4:c.173+604G>A	ENSP00000346969.4:n.173+604G>A
ENST00000394971.7:c.267+282G>A	ENSP00000378422.3:n.267+282G>A
ENST00000394975.2:c.174-532G>A	ENSP00000378426.2:n.174-532G>A
ENST00000420057.2:c.245+1436G>A
ENST00000498155.1:c.271-532G>A	ENSP00000417662.1:n.271-532G>A
ENST00000529564.1:c.174-532G>A	ENSP00000431371.1:n.174-532G>A
ENST00000532364.1:c.173+604G>A	ENSP00000460316.1:n.173+604G>A
ENST00000533518.5:c.47-532G>A
NM_001311311.1:c.174-532G>A	NP_001298240.1:n.174-532G>A
NM_024006.4:c.174-532G>A	NP_076869.1:n.174-532G>A
NM_024006.5:c.174-532G>A	NP_076869.1:n.174-532G>A
NM_206824.1:c.173+604G>A	NP_996560.1:n.173+604G>A
NM_206824.2:c.173+604G>A	NP_996560.1:n.173+604G>A
XM_011545944.1:c.174-532G>A	XP_011544246.1:n.174-532G>A
XM_011545945.1:c.173+604G>A	XP_011544247.1:n.173+604G>A
XR_950848.1:n.962-532G>A
NM_024006.6:c.174-532G>A MANE Select	NP_076869.1:n.174-532G>A
NM_001311311.2:c.174-532G>A	NP_001298240.1:n.174-532G>A
NM_206824.3:c.173+604G>A	NP_996560.1:n.173+604G>A