Canonical Allele Identifier: CA449779110

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890888C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923111C>T , CM000668.2:g.30923111C>T	GRCh38
NC_000006.11:g.30890888C>T , CM000668.1:g.30890888C>T	GRCh37
NC_000006.10:g.30998867C>T	NCBI36
NG_034224.1:g.13904C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2193C>T	ENSP00000441000.2:p.Asp731=
ENST00000672801.1:c.2187C>T	ENSP00000500615.1:p.Asp729=
ENST00000676266.1:c.2193C>T MANE Select	ENSP00000502585.1:p.Asp731=
ENST00000321897.9:c.2193C>T	ENSP00000316092.5:p.Asp731=
ENST00000469358.5:n.2181C>T
ENST00000476162.5:n.980C>T
ENST00000477052.1:n.279C>T
ENST00000477288.5:n.4806C>T
ENST00000541562.5:c.2283C>T	ENSP00000441000.1:p.Asp761=
ENST00000542001.5:c.2187C>T	ENSP00000438200.2:p.Asp729=
ENST00000625423.2:c.1773C>T	ENSP00000485818.1:p.Asp591=
NM_001167733.2:c.1773C>T	NP_001161205.1:p.Asp591=
NM_001167734.1:c.2283C>T	NP_001161206.1:p.Asp761=
NM_020442.5:c.2193C>T	NP_065175.4:p.Asp731=
NM_001167733.3:c.1773C>T	NP_001161205.1:p.Asp591=
NM_001167734.2:c.2283C>T	NP_001161206.1:p.Asp761=
NM_020442.6:c.2193C>T MANE Select	NP_065175.4:p.Asp731=