Canonical Allele Identifier: CA8021105
Gene: VKORC1 HGNC NCBI

Linked Data

dbSNP Id: rs748397246

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091083C>T , CM000678.2:g.31091083C>T GRCh38
NC_000016.9:g.31102404C>T , CM000678.1:g.31102404C>T GRCh37
NC_000016.8:g.31009905C>T NCBI36
NG_011564.1:g.8873G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.*51G>A MANE Select ENSP00000378426.2:n.*51G>A
ENST00000300851.10:c.*154G>A ENSP00000300851.6:n.*154G>A
ENST00000319788.11:c.*154G>A ENSP00000326135.7:n.*154G>A
ENST00000354895.4:c.*154G>A ENSP00000346969.4:n.*154G>A
ENST00000394975.2:c.*51G>A ENSP00000378426.2:n.*51G>A
ENST00000420057.2:c.505G>A
ENST00000529564.1:c.283+2229G>A ENSP00000431371.1:n.283+2229G>A
ENST00000532364.1:c.173+3474G>A ENSP00000460316.1:n.173+3474G>A
ENST00000533518.5:c.407+9G>A
NM_001311311.1:c.*51G>A NP_001298240.1:n.*51G>A
NM_024006.4:c.*51G>A NP_076869.1:n.*51G>A
NM_024006.5:c.*51G>A NP_076869.1:n.*51G>A
NM_206824.1:c.*154G>A NP_996560.1:n.*154G>A
NM_206824.2:c.*154G>A NP_996560.1:n.*154G>A
XM_011545944.1:c.*51G>A XP_011544246.1:n.*51G>A
XM_011545945.1:c.*154G>A XP_011544247.1:n.*154G>A
XR_950848.1:n.1331G>A
NM_024006.6:c.*51G>A MANE Select NP_076869.1:n.*51G>A
NM_001311311.2:c.*51G>A NP_001298240.1:n.*51G>A
NM_206824.3:c.*154G>A NP_996560.1:n.*154G>A