Canonical Allele Identifier: CA363174882

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890684T>G (hg19) ; chr6:g.30922907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922907T>G , CM000668.2:g.30922907T>G	GRCh38
NC_000006.11:g.30890684T>G , CM000668.1:g.30890684T>G	GRCh37
NC_000006.10:g.30998663T>G	NCBI36
NG_034224.1:g.13700T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2116T>G	ENSP00000441000.2:p.Phe706Val
ENST00000672801.1:c.2110T>G	ENSP00000500615.1:p.Phe704Val
ENST00000676266.1:c.2116T>G MANE Select	ENSP00000502585.1:p.Phe706Val
ENST00000321897.9:c.2116T>G	ENSP00000316092.5:p.Phe706Val
ENST00000469358.5:n.2104T>G
ENST00000476162.5:n.903T>G
ENST00000477052.1:n.202T>G
ENST00000477288.5:n.4729T>G
ENST00000541562.5:c.2206T>G	ENSP00000441000.1:p.Phe736Val
ENST00000542001.5:c.2110T>G	ENSP00000438200.2:p.Phe704Val
ENST00000625423.2:c.1696T>G	ENSP00000485818.1:p.Phe566Val
NM_001167733.2:c.1696T>G	NP_001161205.1:p.Phe566Val
NM_001167734.1:c.2206T>G	NP_001161206.1:p.Phe736Val
NM_020442.5:c.2116T>G	NP_065175.4:p.Phe706Val
NM_001167733.3:c.1696T>G	NP_001161205.1:p.Phe566Val
NM_001167734.2:c.2206T>G	NP_001161206.1:p.Phe736Val
NM_020442.6:c.2116T>G MANE Select	NP_065175.4:p.Phe706Val