Canonical Allele Identifier: CA3706156

Gene: VARS2

Linked Data

• dbSNP Id: rs754381626
• ExAC: 6:30890544 C / T
• gnomAD v2: 6-30890544-C-T
• gnomAD v4: 6-30922767-C-T
• MyVariant Identifiers: chr6:g.30890544C>T (hg19) ; chr6:g.30922767C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922767C>T , CM000668.2:g.30922767C>T	GRCh38
NC_000006.11:g.30890544C>T , CM000668.1:g.30890544C>T	GRCh37
NC_000006.10:g.30998523C>T	NCBI36
NG_034224.1:g.13560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2099C>T	ENSP00000441000.2:p.Ala700Val
ENST00000672801.1:c.2093C>T	ENSP00000500615.1:p.Ala698Val
ENST00000676266.1:c.2099C>T MANE Select	ENSP00000502585.1:p.Ala700Val
ENST00000321897.9:c.2099C>T	ENSP00000316092.5:p.Ala700Val
ENST00000469358.5:n.2087C>T
ENST00000476162.5:n.886C>T
ENST00000477052.1:n.185C>T
ENST00000477288.5:n.4712C>T
ENST00000541562.5:c.2189C>T	ENSP00000441000.1:p.Ala730Val
ENST00000542001.5:c.2093C>T	ENSP00000438200.2:p.Ala698Val
ENST00000625423.2:c.1679C>T	ENSP00000485818.1:p.Ala560Val
NM_001167733.2:c.1679C>T	NP_001161205.1:p.Ala560Val
NM_001167734.1:c.2189C>T	NP_001161206.1:p.Ala730Val
NM_020442.5:c.2099C>T	NP_065175.4:p.Ala700Val
NM_001167733.3:c.1679C>T	NP_001161205.1:p.Ala560Val
NM_001167734.2:c.2189C>T	NP_001161206.1:p.Ala730Val
NM_020442.6:c.2099C>T MANE Select	NP_065175.4:p.Ala700Val