Canonical Allele Identifier: CA363175130

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890921C>G (hg19) ; chr6:g.30923144C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923144C>G , CM000668.2:g.30923144C>G	GRCh38
NC_000006.11:g.30890921C>G , CM000668.1:g.30890921C>G	GRCh37
NC_000006.10:g.30998900C>G	NCBI36
NG_034224.1:g.13937C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2226C>G	ENSP00000441000.2:p.Cys742Trp
ENST00000672801.1:c.2220C>G	ENSP00000500615.1:p.Cys740Trp
ENST00000676266.1:c.2226C>G MANE Select	ENSP00000502585.1:p.Cys742Trp
ENST00000321897.9:c.2226C>G	ENSP00000316092.5:p.Cys742Trp
ENST00000469358.5:n.2214C>G
ENST00000476162.5:n.1013C>G
ENST00000477052.1:n.312C>G
ENST00000477288.5:n.4839C>G
ENST00000541562.5:c.2316C>G	ENSP00000441000.1:p.Cys772Trp
ENST00000542001.5:c.2220C>G	ENSP00000438200.2:p.Cys740Trp
ENST00000625423.2:c.1806C>G	ENSP00000485818.1:p.Cys602Trp
NM_001167733.2:c.1806C>G	NP_001161205.1:p.Cys602Trp
NM_001167734.1:c.2316C>G	NP_001161206.1:p.Cys772Trp
NM_020442.5:c.2226C>G	NP_065175.4:p.Cys742Trp
NM_001167733.3:c.1806C>G	NP_001161205.1:p.Cys602Trp
NM_001167734.2:c.2316C>G	NP_001161206.1:p.Cys772Trp
NM_020442.6:c.2226C>G MANE Select	NP_065175.4:p.Cys742Trp