Canonical Allele Identifier: CA16622109
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 425575
ClinVar RCV Id: RCV000488719
dbSNP Id: rs1085307141

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17230709A>G , CM000672.2:g.17230709A>G GRCh38
NC_000010.10:g.17272708A>G , CM000672.1:g.17272708A>G GRCh37
NC_000010.9:g.17312714A>G NCBI36
NG_012413.1:g.7451A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000544301.7:c.623A>G MANE Select ENSP00000446007.1:p.Gln208Arg
ENST00000637053.1:n.56A>G
ENST00000224237.9:c.623A>G ENSP00000224237.5:p.Gln208Arg
ENST00000421459.2:c.101A>G ENSP00000391842.2:p.Gln34Arg
ENST00000469543.5:c.77A>G ENSP00000431702.1:p.Gln26Arg
ENST00000485947.1:n.755A>G
ENST00000487938.5:c.623A>G ENSP00000435613.1:p.Gln208Arg
ENST00000544301.5:c.623A>G ENSP00000446007.1:p.Gln208Arg
NM_003380.3:c.623A>G NP_003371.2:p.Gln208Arg
XM_006717500.1:c.623A>G XP_006717563.1:p.Gln208Arg
XM_011519649.1:c.623A>G XP_011517951.1:p.Gln208Arg
NM_003380.4:c.623A>G NP_003371.2:p.Gln208Arg
XM_006717500.2:c.623A>G XP_006717563.1:p.Gln208Arg
NM_003380.5:c.623A>G MANE Select NP_003371.2:p.Gln208Arg