Canonical Allele Identifier: CA2632821407
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091019G>T , CM000678.2:g.31091019G>T GRCh38
NC_000016.9:g.31102340G>T , CM000678.1:g.31102340G>T GRCh37
NC_000016.8:g.31009841G>T NCBI36
NG_011564.1:g.8937C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*115C>A MANE Select ENSP00000378426.2:n.*115C>A
ENST00000300851.10:c.*218C>A ENSP00000300851.6:n.*218C>A
ENST00000319788.11:c.*218C>A ENSP00000326135.7:n.*218C>A
ENST00000354895.4:c.*218C>A ENSP00000346969.4:n.*218C>A
ENST00000394975.2:c.*115C>A ENSP00000378426.2:n.*115C>A
ENST00000420057.2:c.569C>A
ENST00000529564.1:c.283+2293C>A ENSP00000431371.1:n.283+2293C>A
ENST00000532364.1:c.173+3538C>A ENSP00000460316.1:n.173+3538C>A
ENST00000533518.5:c.407+73C>A
NM_001311311.1:c.*115C>A NP_001298240.1:n.*115C>A
NM_024006.4:c.*115C>A NP_076869.1:n.*115C>A
NM_024006.5:c.*115C>A NP_076869.1:n.*115C>A
NM_206824.1:c.*218C>A NP_996560.1:n.*218C>A
NM_206824.2:c.*218C>A NP_996560.1:n.*218C>A
XM_011545944.1:c.*115C>A XP_011544246.1:n.*115C>A
XM_011545945.1:c.*218C>A XP_011544247.1:n.*218C>A
XR_950848.1:n.1395C>A
NM_024006.6:c.*115C>A MANE Select NP_076869.1:n.*115C>A
NM_001311311.2:c.*115C>A NP_001298240.1:n.*115C>A
NM_206824.3:c.*218C>A NP_996560.1:n.*218C>A