Canonical Allele Identifier: CA363174990
Gene: VARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30922958T>G , CM000668.2:g.30922958T>G GRCh38
NC_000006.11:g.30890735T>G , CM000668.1:g.30890735T>G GRCh37
NC_000006.10:g.30998714T>G NCBI36
NG_034224.1:g.13751T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000541562.6:c.2167T>G ENSP00000441000.2:p.Cys723Gly
ENST00000672801.1:c.2161T>G ENSP00000500615.1:p.Cys721Gly
ENST00000676266.1:c.2167T>G MANE Select ENSP00000502585.1:p.Cys723Gly
ENST00000321897.9:c.2167T>G ENSP00000316092.5:p.Cys723Gly
ENST00000469358.5:n.2155T>G
ENST00000476162.5:n.954T>G
ENST00000477052.1:n.253T>G
ENST00000477288.5:n.4780T>G
ENST00000541562.5:c.2257T>G ENSP00000441000.1:p.Cys753Gly
ENST00000542001.5:c.2161T>G ENSP00000438200.2:p.Cys721Gly
ENST00000625423.2:c.1747T>G ENSP00000485818.1:p.Cys583Gly
NM_001167733.2:c.1747T>G NP_001161205.1:p.Cys583Gly
NM_001167734.1:c.2257T>G NP_001161206.1:p.Cys753Gly
NM_020442.5:c.2167T>G NP_065175.4:p.Cys723Gly
NM_001167733.3:c.1747T>G NP_001161205.1:p.Cys583Gly
NM_001167734.2:c.2257T>G NP_001161206.1:p.Cys753Gly
NM_020442.6:c.2167T>G MANE Select NP_065175.4:p.Cys723Gly