Canonical Allele Identifier: CA2632821382
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091007G>T , CM000678.2:g.31091007G>T GRCh38
NC_000016.9:g.31102328G>T , CM000678.1:g.31102328G>T GRCh37
NC_000016.8:g.31009829G>T NCBI36
NG_011564.1:g.8949C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*127C>A MANE Select ENSP00000378426.2:n.*127C>A
ENST00000300851.10:c.*230C>A ENSP00000300851.6:n.*230C>A
ENST00000319788.11:c.*230C>A ENSP00000326135.7:n.*230C>A
ENST00000354895.4:c.*230C>A ENSP00000346969.4:n.*230C>A
ENST00000394975.2:c.*127C>A ENSP00000378426.2:n.*127C>A
ENST00000420057.2:c.581C>A
ENST00000529564.1:c.283+2305C>A ENSP00000431371.1:n.283+2305C>A
ENST00000532364.1:c.173+3550C>A ENSP00000460316.1:n.173+3550C>A
ENST00000533518.5:c.407+85C>A
NM_001311311.1:c.*127C>A NP_001298240.1:n.*127C>A
NM_024006.4:c.*127C>A NP_076869.1:n.*127C>A
NM_024006.5:c.*127C>A NP_076869.1:n.*127C>A
NM_206824.1:c.*230C>A NP_996560.1:n.*230C>A
NM_206824.2:c.*230C>A NP_996560.1:n.*230C>A
XM_011545944.1:c.*127C>A XP_011544246.1:n.*127C>A
XM_011545945.1:c.*230C>A XP_011544247.1:n.*230C>A
XR_950848.1:n.1407C>A
NM_024006.6:c.*127C>A MANE Select NP_076869.1:n.*127C>A
NM_001311311.2:c.*127C>A NP_001298240.1:n.*127C>A
NM_206824.3:c.*230C>A NP_996560.1:n.*230C>A