Canonical Allele Identifier: CA449779211

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890545A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922768A>T , CM000668.2:g.30922768A>T	GRCh38
NC_000006.11:g.30890545A>T , CM000668.1:g.30890545A>T	GRCh37
NC_000006.10:g.30998524A>T	NCBI36
NG_034224.1:g.13561A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2100A>T	ENSP00000441000.2:p.Ala700=
ENST00000672801.1:c.2094A>T	ENSP00000500615.1:p.Ala698=
ENST00000676266.1:c.2100A>T MANE Select	ENSP00000502585.1:p.Ala700=
ENST00000321897.9:c.2100A>T	ENSP00000316092.5:p.Ala700=
ENST00000469358.5:n.2088A>T
ENST00000476162.5:n.887A>T
ENST00000477052.1:n.186A>T
ENST00000477288.5:n.4713A>T
ENST00000541562.5:c.2190A>T	ENSP00000441000.1:p.Ala730=
ENST00000542001.5:c.2094A>T	ENSP00000438200.2:p.Ala698=
ENST00000625423.2:c.1680A>T	ENSP00000485818.1:p.Ala560=
NM_001167733.2:c.1680A>T	NP_001161205.1:p.Ala560=
NM_001167734.1:c.2190A>T	NP_001161206.1:p.Ala730=
NM_020442.5:c.2100A>T	NP_065175.4:p.Ala700=
NM_001167733.3:c.1680A>T	NP_001161205.1:p.Ala560=
NM_001167734.2:c.2190A>T	NP_001161206.1:p.Ala730=
NM_020442.6:c.2100A>T MANE Select	NP_065175.4:p.Ala700=