Canonical Allele Identifier: CA280619680
Gene: VKORC1 HGNC NCBI

Linked Data

dbSNP Id: rs1034842844

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31090973G>A , CM000678.2:g.31090973G>A GRCh38
NC_000016.9:g.31102294G>A , CM000678.1:g.31102294G>A GRCh37
NC_000016.8:g.31009795G>A NCBI36
NG_011564.1:g.8983C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.*161C>T MANE Select ENSP00000378426.2:n.*161C>T
ENST00000300851.10:c.*264C>T ENSP00000300851.6:n.*264C>T
ENST00000319788.11:c.*264C>T ENSP00000326135.7:n.*264C>T
ENST00000354895.4:c.*264C>T ENSP00000346969.4:n.*264C>T
ENST00000394975.2:c.*161C>T ENSP00000378426.2:n.*161C>T
ENST00000420057.2:c.615C>T
ENST00000529564.1:c.283+2339C>T ENSP00000431371.1:n.283+2339C>T
ENST00000532364.1:c.173+3584C>T ENSP00000460316.1:n.173+3584C>T
ENST00000533518.5:c.407+119C>T
NM_001311311.1:c.*161C>T NP_001298240.1:n.*161C>T
NM_024006.4:c.*161C>T NP_076869.1:n.*161C>T
NM_024006.5:c.*161C>T NP_076869.1:n.*161C>T
NM_206824.1:c.*264C>T NP_996560.1:n.*264C>T
NM_206824.2:c.*264C>T NP_996560.1:n.*264C>T
XM_011545944.1:c.*161C>T XP_011544246.1:n.*161C>T
XM_011545945.1:c.*264C>T XP_011544247.1:n.*264C>T
XR_950848.1:n.1441C>T
NM_024006.6:c.*161C>T MANE Select NP_076869.1:n.*161C>T
NM_001311311.2:c.*161C>T NP_001298240.1:n.*161C>T
NM_206824.3:c.*264C>T NP_996560.1:n.*264C>T