Canonical Allele Identifier: CA3706231

Gene: VARS2

Linked Data

• dbSNP Id: rs775750497
• ExAC: 6:30891034 A / G
• gnomAD v2: 6-30891034-A-G
• MyVariant Identifiers: chr6:g.30891034A>G (hg19) ; chr6:g.30923257A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923257A>G , CM000668.2:g.30923257A>G	GRCh38
NC_000006.11:g.30891034A>G , CM000668.1:g.30891034A>G	GRCh37
NC_000006.10:g.30999013A>G	NCBI36
NG_034224.1:g.14050A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2313+26A>G	ENSP00000441000.2:n.2313+26A>G
ENST00000672801.1:c.2307+26A>G	ENSP00000500615.1:n.2307+26A>G
ENST00000676266.1:c.2313+26A>G MANE Select	ENSP00000502585.1:n.2313+26A>G
ENST00000321897.9:c.2313+26A>G	ENSP00000316092.5:n.2313+26A>G
ENST00000469358.5:n.2301+26A>G
ENST00000473916.1:n.24+26A>G
ENST00000476162.5:n.1100+26A>G
ENST00000477052.1:n.399+26A>G
ENST00000477288.5:n.4926+26A>G
ENST00000541562.5:c.2403+26A>G	ENSP00000441000.1:n.2403+26A>G
ENST00000542001.5:c.2307+26A>G	ENSP00000438200.2:n.2307+26A>G
ENST00000625423.2:c.1893+26A>G	ENSP00000485818.1:n.1893+26A>G
NM_001167733.2:c.1893+26A>G	NP_001161205.1:n.1893+26A>G
NM_001167734.1:c.2403+26A>G	NP_001161206.1:n.2403+26A>G
NM_020442.5:c.2313+26A>G	NP_065175.4:n.2313+26A>G
NM_001167733.3:c.1893+26A>G	NP_001161205.1:n.1893+26A>G
NM_001167734.2:c.2403+26A>G	NP_001161206.1:n.2403+26A>G
NM_020442.6:c.2313+26A>G MANE Select	NP_065175.4:n.2313+26A>G