Canonical Allele Identifier: CA363175095

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890907G>C (hg19) ; chr6:g.30923130G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923130G>C , CM000668.2:g.30923130G>C	GRCh38
NC_000006.11:g.30890907G>C , CM000668.1:g.30890907G>C	GRCh37
NC_000006.10:g.30998886G>C	NCBI36
NG_034224.1:g.13923G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2212G>C	ENSP00000441000.2:p.Glu738Gln
ENST00000672801.1:c.2206G>C	ENSP00000500615.1:p.Glu736Gln
ENST00000676266.1:c.2212G>C MANE Select	ENSP00000502585.1:p.Glu738Gln
ENST00000321897.9:c.2212G>C	ENSP00000316092.5:p.Glu738Gln
ENST00000469358.5:n.2200G>C
ENST00000476162.5:n.999G>C
ENST00000477052.1:n.298G>C
ENST00000477288.5:n.4825G>C
ENST00000541562.5:c.2302G>C	ENSP00000441000.1:p.Glu768Gln
ENST00000542001.5:c.2206G>C	ENSP00000438200.2:p.Glu736Gln
ENST00000625423.2:c.1792G>C	ENSP00000485818.1:p.Glu598Gln
NM_001167733.2:c.1792G>C	NP_001161205.1:p.Glu598Gln
NM_001167734.1:c.2302G>C	NP_001161206.1:p.Glu768Gln
NM_020442.5:c.2212G>C	NP_065175.4:p.Glu738Gln
NM_001167733.3:c.1792G>C	NP_001161205.1:p.Glu598Gln
NM_001167734.2:c.2302G>C	NP_001161206.1:p.Glu768Gln
NM_020442.6:c.2212G>C MANE Select	NP_065175.4:p.Glu738Gln