Canonical Allele Identifier: CA2677908869

Gene: VARS2

Linked Data

• gnomAD v4: 6-30922839-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922839A>G , CM000668.2:g.30922839A>G	GRCh38
NC_000006.11:g.30890616A>G , CM000668.1:g.30890616A>G	GRCh37
NC_000006.10:g.30998595A>G	NCBI36
NG_034224.1:g.13632A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2107-59A>G	ENSP00000441000.2:n.2107-59A>G
ENST00000672801.1:c.2101-59A>G	ENSP00000500615.1:n.2101-59A>G
ENST00000676266.1:c.2107-59A>G MANE Select	ENSP00000502585.1:n.2107-59A>G
ENST00000321897.9:c.2107-59A>G	ENSP00000316092.5:n.2107-59A>G
ENST00000469358.5:n.2095-59A>G
ENST00000476162.5:n.894-59A>G
ENST00000477052.1:n.193-59A>G
ENST00000477288.5:n.4720-59A>G
ENST00000541562.5:c.2197-59A>G	ENSP00000441000.1:n.2197-59A>G
ENST00000542001.5:c.2101-59A>G	ENSP00000438200.2:n.2101-59A>G
ENST00000625423.2:c.1687-59A>G	ENSP00000485818.1:n.1687-59A>G
NM_001167733.2:c.1687-59A>G	NP_001161205.1:n.1687-59A>G
NM_001167734.1:c.2197-59A>G	NP_001161206.1:n.2197-59A>G
NM_020442.5:c.2107-59A>G	NP_065175.4:n.2107-59A>G
NM_001167733.3:c.1687-59A>G	NP_001161205.1:n.1687-59A>G
NM_001167734.2:c.2197-59A>G	NP_001161206.1:n.2197-59A>G
NM_020442.6:c.2107-59A>G MANE Select	NP_065175.4:n.2107-59A>G