Canonical Allele Identifier: CA449779232

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890710G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922933G>C , CM000668.2:g.30922933G>C	GRCh38
NC_000006.11:g.30890710G>C , CM000668.1:g.30890710G>C	GRCh37
NC_000006.10:g.30998689G>C	NCBI36
NG_034224.1:g.13726G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2142G>C	ENSP00000441000.2:p.Gly714=
ENST00000672801.1:c.2136G>C	ENSP00000500615.1:p.Gly712=
ENST00000676266.1:c.2142G>C MANE Select	ENSP00000502585.1:p.Gly714=
ENST00000321897.9:c.2142G>C	ENSP00000316092.5:p.Gly714=
ENST00000469358.5:n.2130G>C
ENST00000476162.5:n.929G>C
ENST00000477052.1:n.228G>C
ENST00000477288.5:n.4755G>C
ENST00000541562.5:c.2232G>C	ENSP00000441000.1:p.Gly744=
ENST00000542001.5:c.2136G>C	ENSP00000438200.2:p.Gly712=
ENST00000625423.2:c.1722G>C	ENSP00000485818.1:p.Gly574=
NM_001167733.2:c.1722G>C	NP_001161205.1:p.Gly574=
NM_001167734.1:c.2232G>C	NP_001161206.1:p.Gly744=
NM_020442.5:c.2142G>C	NP_065175.4:p.Gly714=
NM_001167733.3:c.1722G>C	NP_001161205.1:p.Gly574=
NM_001167734.2:c.2232G>C	NP_001161206.1:p.Gly744=
NM_020442.6:c.2142G>C MANE Select	NP_065175.4:p.Gly714=