Canonical Allele Identifier: CA449779118
Gene: VARS2 HGNC NCBI

Linked Data

dbSNP Id: rs1440838382
gnomAD v2: 6-30890900-A-G
gnomAD v3: 6-30923123-A-G
gnomAD v4: 6-30923123-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30923123A>G , CM000668.2:g.30923123A>G GRCh38
NC_000006.11:g.30890900A>G , CM000668.1:g.30890900A>G GRCh37
NC_000006.10:g.30998879A>G NCBI36
NG_034224.1:g.13916A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000541562.6:c.2205A>G ENSP00000441000.2:p.Ser735=
ENST00000672801.1:c.2199A>G ENSP00000500615.1:p.Ser733=
ENST00000676266.1:c.2205A>G MANE Select ENSP00000502585.1:p.Ser735=
ENST00000321897.9:c.2205A>G ENSP00000316092.5:p.Ser735=
ENST00000469358.5:n.2193A>G
ENST00000476162.5:n.992A>G
ENST00000477052.1:n.291A>G
ENST00000477288.5:n.4818A>G
ENST00000541562.5:c.2295A>G ENSP00000441000.1:p.Ser765=
ENST00000542001.5:c.2199A>G ENSP00000438200.2:p.Ser733=
ENST00000625423.2:c.1785A>G ENSP00000485818.1:p.Ser595=
NM_001167733.2:c.1785A>G NP_001161205.1:p.Ser595=
NM_001167734.1:c.2295A>G NP_001161206.1:p.Ser765=
NM_020442.5:c.2205A>G NP_065175.4:p.Ser735=
NM_001167733.3:c.1785A>G NP_001161205.1:p.Ser595=
NM_001167734.2:c.2295A>G NP_001161206.1:p.Ser765=
NM_020442.6:c.2205A>G MANE Select NP_065175.4:p.Ser735=