Canonical Allele Identifier: CA363168204

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30883962G>C (hg19) ; chr6:g.30916185G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30916185G>C , CM000668.2:g.30916185G>C	GRCh38
NC_000006.11:g.30883962G>C , CM000668.1:g.30883962G>C	GRCh37
NC_000006.10:g.30991941G>C	NCBI36
NG_034224.1:g.6978G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.607G>C	ENSP00000441000.2:p.Gly203Arg
ENST00000672801.1:c.607G>C	ENSP00000500615.1:p.Gly203Arg
ENST00000676266.1:c.607G>C MANE Select	ENSP00000502585.1:p.Gly203Arg
ENST00000321897.9:c.607G>C	ENSP00000316092.5:p.Gly203Arg
ENST00000428017.5:c.607G>C	ENSP00000403749.1:p.Gly203Arg
ENST00000467717.5:n.485G>C
ENST00000477288.5:n.3195G>C
ENST00000541562.5:c.697G>C	ENSP00000441000.1:p.Gly233Arg
ENST00000542001.5:c.607G>C	ENSP00000438200.2:p.Gly203Arg
ENST00000625423.2:c.187G>C	ENSP00000485818.1:p.Gly63Arg
NM_001167733.2:c.187G>C	NP_001161205.1:p.Gly63Arg
NM_001167734.1:c.697G>C	NP_001161206.1:p.Gly233Arg
NM_020442.5:c.607G>C	NP_065175.4:p.Gly203Arg
NM_001167733.3:c.187G>C	NP_001161205.1:p.Gly63Arg
NM_001167734.2:c.697G>C	NP_001161206.1:p.Gly233Arg
NM_020442.6:c.607G>C MANE Select	NP_065175.4:p.Gly203Arg