Canonical Allele Identifier: CA363174835

Gene: VARS2

Linked Data

• gnomAD v4: 6-30922770-C-T
• MyVariant Identifiers: chr6:g.30890547C>T (hg19) ; chr6:g.30922770C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922770C>T , CM000668.2:g.30922770C>T	GRCh38
NC_000006.11:g.30890547C>T , CM000668.1:g.30890547C>T	GRCh37
NC_000006.10:g.30998526C>T	NCBI36
NG_034224.1:g.13563C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2102C>T	ENSP00000441000.2:p.Ala701Val
ENST00000672801.1:c.2096C>T	ENSP00000500615.1:p.Ala699Val
ENST00000676266.1:c.2102C>T MANE Select	ENSP00000502585.1:p.Ala701Val
ENST00000321897.9:c.2102C>T	ENSP00000316092.5:p.Ala701Val
ENST00000469358.5:n.2090C>T
ENST00000476162.5:n.889C>T
ENST00000477052.1:n.188C>T
ENST00000477288.5:n.4715C>T
ENST00000541562.5:c.2192C>T	ENSP00000441000.1:p.Ala731Val
ENST00000542001.5:c.2096C>T	ENSP00000438200.2:p.Ala699Val
ENST00000625423.2:c.1682C>T	ENSP00000485818.1:p.Ala561Val
NM_001167733.2:c.1682C>T	NP_001161205.1:p.Ala561Val
NM_001167734.1:c.2192C>T	NP_001161206.1:p.Ala731Val
NM_020442.5:c.2102C>T	NP_065175.4:p.Ala701Val
NM_001167733.3:c.1682C>T	NP_001161205.1:p.Ala561Val
NM_001167734.2:c.2192C>T	NP_001161206.1:p.Ala731Val
NM_020442.6:c.2102C>T MANE Select	NP_065175.4:p.Ala701Val