Canonical Allele Identifier: CA823854611

Gene: VARS2

Linked Data

• dbSNP Id: rs1349592111
• gnomAD v4: 6-30922837-C-A
• MyVariant Identifiers: chr6:g.30890614C>A (hg19) ; chr6:g.30922837C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922837C>A , CM000668.2:g.30922837C>A	GRCh38
NC_000006.11:g.30890614C>A , CM000668.1:g.30890614C>A	GRCh37
NC_000006.10:g.30998593C>A	NCBI36
NG_034224.1:g.13630C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2107-61C>A	ENSP00000441000.2:n.2107-61C>A
ENST00000672801.1:c.2101-61C>A	ENSP00000500615.1:n.2101-61C>A
ENST00000676266.1:c.2107-61C>A MANE Select	ENSP00000502585.1:n.2107-61C>A
ENST00000321897.9:c.2107-61C>A	ENSP00000316092.5:n.2107-61C>A
ENST00000469358.5:n.2095-61C>A
ENST00000476162.5:n.894-61C>A
ENST00000477052.1:n.193-61C>A
ENST00000477288.5:n.4720-61C>A
ENST00000541562.5:c.2197-61C>A	ENSP00000441000.1:n.2197-61C>A
ENST00000542001.5:c.2101-61C>A	ENSP00000438200.2:n.2101-61C>A
ENST00000625423.2:c.1687-61C>A	ENSP00000485818.1:n.1687-61C>A
NM_001167733.2:c.1687-61C>A	NP_001161205.1:n.1687-61C>A
NM_001167734.1:c.2197-61C>A	NP_001161206.1:n.2197-61C>A
NM_020442.5:c.2107-61C>A	NP_065175.4:n.2107-61C>A
NM_001167733.3:c.1687-61C>A	NP_001161205.1:n.1687-61C>A
NM_001167734.2:c.2197-61C>A	NP_001161206.1:n.2197-61C>A
NM_020442.6:c.2107-61C>A MANE Select	NP_065175.4:n.2107-61C>A