Canonical Allele Identifier: CA2632821252
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31090929T>G , CM000678.2:g.31090929T>G GRCh38
NC_000016.9:g.31102250T>G , CM000678.1:g.31102250T>G GRCh37
NC_000016.8:g.31009751T>G NCBI36
NG_011564.1:g.9027A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*205A>C MANE Select ENSP00000378426.2:n.*205A>C
ENST00000300851.10:c.*308A>C ENSP00000300851.6:n.*308A>C
ENST00000319788.11:c.*308A>C ENSP00000326135.7:n.*308A>C
ENST00000354895.4:c.*308A>C ENSP00000346969.4:n.*308A>C
ENST00000394975.2:c.*205A>C ENSP00000378426.2:n.*205A>C
ENST00000420057.2:c.659A>C
ENST00000529564.1:c.283+2383A>C ENSP00000431371.1:n.283+2383A>C
ENST00000532364.1:c.173+3628A>C ENSP00000460316.1:n.173+3628A>C
ENST00000533518.5:c.407+163A>C
NM_001311311.1:c.*205A>C NP_001298240.1:n.*205A>C
NM_024006.4:c.*205A>C NP_076869.1:n.*205A>C
NM_024006.5:c.*205A>C NP_076869.1:n.*205A>C
NM_206824.1:c.*308A>C NP_996560.1:n.*308A>C
NM_206824.2:c.*308A>C NP_996560.1:n.*308A>C
XM_011545944.1:c.*205A>C XP_011544246.1:n.*205A>C
XM_011545945.1:c.*308A>C XP_011544247.1:n.*308A>C
XR_950848.1:n.1485A>C
NM_024006.6:c.*205A>C MANE Select NP_076869.1:n.*205A>C
NM_001311311.2:c.*205A>C NP_001298240.1:n.*205A>C
NM_206824.3:c.*308A>C NP_996560.1:n.*308A>C