Canonical Allele Identifier: CA395732522
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31094564A>T , CM000678.2:g.31094564A>T GRCh38
NC_000016.9:g.31105885A>T , CM000678.1:g.31105885A>T GRCh37
NC_000016.8:g.31013386A>T NCBI36
NG_011564.1:g.5392T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.166T>A MANE Select ENSP00000378426.2:p.Ser56Thr
ENST00000300851.10:c.166T>A ENSP00000300851.6:p.Ser56Thr
ENST00000319788.11:c.166T>A ENSP00000326135.7:p.Ser56Thr
ENST00000354895.4:c.166T>A ENSP00000346969.4:p.Ser56Thr
ENST00000394975.2:c.166T>A ENSP00000378426.2:p.Ser56Thr
ENST00000420057.2:c.245+825T>A
ENST00000498155.1:c.270+825T>A ENSP00000417662.1:n.270+825T>A
ENST00000529564.1:c.166T>A ENSP00000431371.1:p.Ser56Thr
ENST00000532364.1:c.166T>A ENSP00000460316.1:p.Ser56Thr
ENST00000533518.5:c.39T>A
NM_001311311.1:c.166T>A NP_001298240.1:p.Ser56Thr
NM_024006.4:c.166T>A NP_076869.1:p.Ser56Thr
NM_024006.5:c.166T>A NP_076869.1:p.Ser56Thr
NM_206824.1:c.166T>A NP_996560.1:p.Ser56Thr
NM_206824.2:c.166T>A NP_996560.1:p.Ser56Thr
XM_011545944.1:c.166T>A XP_011544246.1:p.Ser56Thr
XM_011545945.1:c.166T>A XP_011544247.1:p.Ser56Thr
XR_950848.1:n.954T>A
NM_024006.6:c.166T>A MANE Select NP_076869.1:p.Ser56Thr
NM_001311311.2:c.166T>A NP_001298240.1:p.Ser56Thr
NM_206824.3:c.166T>A NP_996560.1:p.Ser56Thr