Canonical Allele Identifier: CA2216888870
Gene: VKORC1 HGNC NCBI

Linked Data

dbSNP Id: rs2057285757

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091090G>A , CM000678.2:g.31091090G>A GRCh38
NC_000016.9:g.31102411G>A , CM000678.1:g.31102411G>A GRCh37
NC_000016.8:g.31009912G>A NCBI36
NG_011564.1:g.8866C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.*44C>T MANE Select ENSP00000378426.2:n.*44C>T
ENST00000300851.10:c.*147C>T ENSP00000300851.6:n.*147C>T
ENST00000319788.11:c.*147C>T ENSP00000326135.7:n.*147C>T
ENST00000354895.4:c.*147C>T ENSP00000346969.4:n.*147C>T
ENST00000394975.2:c.*44C>T ENSP00000378426.2:n.*44C>T
ENST00000420057.2:c.498C>T
ENST00000529564.1:c.283+2222C>T ENSP00000431371.1:n.283+2222C>T
ENST00000532364.1:c.173+3467C>T ENSP00000460316.1:n.173+3467C>T
ENST00000533518.5:c.407+2C>T
NM_001311311.1:c.*44C>T NP_001298240.1:n.*44C>T
NM_024006.4:c.*44C>T NP_076869.1:n.*44C>T
NM_024006.5:c.*44C>T NP_076869.1:n.*44C>T
NM_206824.1:c.*147C>T NP_996560.1:n.*147C>T
NM_206824.2:c.*147C>T NP_996560.1:n.*147C>T
XM_011545944.1:c.*44C>T XP_011544246.1:n.*44C>T
XM_011545945.1:c.*147C>T XP_011544247.1:n.*147C>T
XR_950848.1:n.1324C>T
NM_024006.6:c.*44C>T MANE Select NP_076869.1:n.*44C>T
NM_001311311.2:c.*44C>T NP_001298240.1:n.*44C>T
NM_206824.3:c.*147C>T NP_996560.1:n.*147C>T