Canonical Allele Identifier: CA2216888631

Gene: VKORC1

Linked Data

• dbSNP Id: rs1010575442
• gnomAD v4: 16-31090966-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090966C>G , CM000678.2:g.31090966C>G	GRCh38
NC_000016.9:g.31102287C>G , CM000678.1:g.31102287C>G	GRCh37
NC_000016.8:g.31009788C>G	NCBI36
NG_011564.1:g.8990G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*168G>C MANE Select	ENSP00000378426.2:n.*168G>C
ENST00000300851.10:c.*271G>C	ENSP00000300851.6:n.*271G>C
ENST00000319788.11:c.*271G>C	ENSP00000326135.7:n.*271G>C
ENST00000354895.4:c.*271G>C	ENSP00000346969.4:n.*271G>C
ENST00000394975.2:c.*168G>C	ENSP00000378426.2:n.*168G>C
ENST00000420057.2:c.622G>C
ENST00000529564.1:c.283+2346G>C	ENSP00000431371.1:n.283+2346G>C
ENST00000532364.1:c.173+3591G>C	ENSP00000460316.1:n.173+3591G>C
ENST00000533518.5:c.407+126G>C
NM_001311311.1:c.*168G>C	NP_001298240.1:n.*168G>C
NM_024006.4:c.*168G>C	NP_076869.1:n.*168G>C
NM_024006.5:c.*168G>C	NP_076869.1:n.*168G>C
NM_206824.1:c.*271G>C	NP_996560.1:n.*271G>C
NM_206824.2:c.*271G>C	NP_996560.1:n.*271G>C
XM_011545944.1:c.*168G>C	XP_011544246.1:n.*168G>C
XM_011545945.1:c.*271G>C	XP_011544247.1:n.*271G>C
XR_950848.1:n.1448G>C
NM_024006.6:c.*168G>C MANE Select	NP_076869.1:n.*168G>C
NM_001311311.2:c.*168G>C	NP_001298240.1:n.*168G>C
NM_206824.3:c.*271G>C	NP_996560.1:n.*271G>C