Canonical Allele Identifier: CA363175227

Gene: VARS2

Linked Data

• MyVariant Identifiers: chr6:g.30890963C>G (hg19) ; chr6:g.30923186C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923186C>G , CM000668.2:g.30923186C>G	GRCh38
NC_000006.11:g.30890963C>G , CM000668.1:g.30890963C>G	GRCh37
NC_000006.10:g.30998942C>G	NCBI36
NG_034224.1:g.13979C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2268C>G	ENSP00000441000.2:p.Ile756Met
ENST00000672801.1:c.2262C>G	ENSP00000500615.1:p.Ile754Met
ENST00000676266.1:c.2268C>G MANE Select	ENSP00000502585.1:p.Ile756Met
ENST00000321897.9:c.2268C>G	ENSP00000316092.5:p.Ile756Met
ENST00000469358.5:n.2256C>G
ENST00000476162.5:n.1055C>G
ENST00000477052.1:n.354C>G
ENST00000477288.5:n.4881C>G
ENST00000541562.5:c.2358C>G	ENSP00000441000.1:p.Ile786Met
ENST00000542001.5:c.2262C>G	ENSP00000438200.2:p.Ile754Met
ENST00000625423.2:c.1848C>G	ENSP00000485818.1:p.Ile616Met
NM_001167733.2:c.1848C>G	NP_001161205.1:p.Ile616Met
NM_001167734.1:c.2358C>G	NP_001161206.1:p.Ile786Met
NM_020442.5:c.2268C>G	NP_065175.4:p.Ile756Met
NM_001167733.3:c.1848C>G	NP_001161205.1:p.Ile616Met
NM_001167734.2:c.2358C>G	NP_001161206.1:p.Ile786Met
NM_020442.6:c.2268C>G MANE Select	NP_065175.4:p.Ile756Met