Canonical Allele Identifier: CA2580576356
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31094032G>T , CM000678.2:g.31094032G>T GRCh38
NC_000016.9:g.31105353G>T , CM000678.1:g.31105353G>T GRCh37
NC_000016.8:g.31012854G>T NCBI36
NG_011564.1:g.5924C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.173+525C>A MANE Select ENSP00000378426.2:n.173+525C>A
ENST00000300851.10:c.173+525C>A ENSP00000300851.6:n.173+525C>A
ENST00000319788.11:c.173+525C>A ENSP00000326135.7:n.173+525C>A
ENST00000354895.4:c.173+525C>A ENSP00000346969.4:n.173+525C>A
ENST00000394971.7:c.267+203C>A ENSP00000378422.3:n.267+203C>A
ENST00000394975.2:c.173+525C>A ENSP00000378426.2:n.173+525C>A
ENST00000420057.2:c.245+1357C>A
ENST00000498155.1:c.271-611C>A ENSP00000417662.1:n.271-611C>A
ENST00000529564.1:c.173+525C>A ENSP00000431371.1:n.173+525C>A
ENST00000532364.1:c.173+525C>A ENSP00000460316.1:n.173+525C>A
ENST00000533518.5:c.46+525C>A
NM_001311311.1:c.173+525C>A NP_001298240.1:n.173+525C>A
NM_024006.4:c.173+525C>A NP_076869.1:n.173+525C>A
NM_024006.5:c.173+525C>A NP_076869.1:n.173+525C>A
NM_206824.1:c.173+525C>A NP_996560.1:n.173+525C>A
NM_206824.2:c.173+525C>A NP_996560.1:n.173+525C>A
XM_011545944.1:c.173+525C>A XP_011544246.1:n.173+525C>A
XM_011545945.1:c.173+525C>A XP_011544247.1:n.173+525C>A
XR_950848.1:n.961+525C>A
NM_024006.6:c.173+525C>A MANE Select NP_076869.1:n.173+525C>A
NM_001311311.2:c.173+525C>A NP_001298240.1:n.173+525C>A
NM_206824.3:c.173+525C>A NP_996560.1:n.173+525C>A