Canonical Allele Identifier: CA363175140

Gene: VARS2

Linked Data

• dbSNP Id: rs1794637259
• gnomAD v4: 6-30923149-A-G
• MyVariant Identifiers: chr6:g.30890926A>G (hg19) ; chr6:g.30923149A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923149A>G , CM000668.2:g.30923149A>G	GRCh38
NC_000006.11:g.30890926A>G , CM000668.1:g.30890926A>G	GRCh37
NC_000006.10:g.30998905A>G	NCBI36
NG_034224.1:g.13942A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2231A>G	ENSP00000441000.2:p.His744Arg
ENST00000672801.1:c.2225A>G	ENSP00000500615.1:p.His742Arg
ENST00000676266.1:c.2231A>G MANE Select	ENSP00000502585.1:p.His744Arg
ENST00000321897.9:c.2231A>G	ENSP00000316092.5:p.His744Arg
ENST00000469358.5:n.2219A>G
ENST00000476162.5:n.1018A>G
ENST00000477052.1:n.317A>G
ENST00000477288.5:n.4844A>G
ENST00000541562.5:c.2321A>G	ENSP00000441000.1:p.His774Arg
ENST00000542001.5:c.2225A>G	ENSP00000438200.2:p.His742Arg
ENST00000625423.2:c.1811A>G	ENSP00000485818.1:p.His604Arg
NM_001167733.2:c.1811A>G	NP_001161205.1:p.His604Arg
NM_001167734.1:c.2321A>G	NP_001161206.1:p.His774Arg
NM_020442.5:c.2231A>G	NP_065175.4:p.His744Arg
NM_001167733.3:c.1811A>G	NP_001161205.1:p.His604Arg
NM_001167734.2:c.2321A>G	NP_001161206.1:p.His774Arg
NM_020442.6:c.2231A>G MANE Select	NP_065175.4:p.His744Arg