Canonical Allele Identifier: CA449779224

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890698C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922921C>A , CM000668.2:g.30922921C>A	GRCh38
NC_000006.11:g.30890698C>A , CM000668.1:g.30890698C>A	GRCh37
NC_000006.10:g.30998677C>A	NCBI36
NG_034224.1:g.13714C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2130C>A	ENSP00000441000.2:p.Ile710=
ENST00000672801.1:c.2124C>A	ENSP00000500615.1:p.Ile708=
ENST00000676266.1:c.2130C>A MANE Select	ENSP00000502585.1:p.Ile710=
ENST00000321897.9:c.2130C>A	ENSP00000316092.5:p.Ile710=
ENST00000469358.5:n.2118C>A
ENST00000476162.5:n.917C>A
ENST00000477052.1:n.216C>A
ENST00000477288.5:n.4743C>A
ENST00000541562.5:c.2220C>A	ENSP00000441000.1:p.Ile740=
ENST00000542001.5:c.2124C>A	ENSP00000438200.2:p.Ile708=
ENST00000625423.2:c.1710C>A	ENSP00000485818.1:p.Ile570=
NM_001167733.2:c.1710C>A	NP_001161205.1:p.Ile570=
NM_001167734.1:c.2220C>A	NP_001161206.1:p.Ile740=
NM_020442.5:c.2130C>A	NP_065175.4:p.Ile710=
NM_001167733.3:c.1710C>A	NP_001161205.1:p.Ile570=
NM_001167734.2:c.2220C>A	NP_001161206.1:p.Ile740=
NM_020442.6:c.2130C>A MANE Select	NP_065175.4:p.Ile710=