Canonical Allele Identifier: CA31541289
Gene: VANGL2 HGNC NCBI

Linked Data

dbSNP Id: rs1023331968
gnomAD v2: 1-160394838-A-G
gnomAD v3: 1-160425048-A-G
gnomAD v4: 1-160425048-A-G
MyVariant Identifiers: chr1:g.160394838A>G (hg19) chr1:g.160425048A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425048A>G , CM000663.2:g.160425048A>G GRCh38
NC_000001.10:g.160394838A>G , CM000663.1:g.160394838A>G GRCh37
NC_000001.9:g.158661462A>G NCBI36
NG_023420.1:g.29475A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-70A>G ENSP00000512747.1:n.1450-70A>G
ENST00000368061.3:c.1306-70A>G MANE Select ENSP00000357040.2:n.1306-70A>G
ENST00000368061.2:c.1306-70A>G ENSP00000357040.2:n.1306-70A>G
NM_020335.2:c.1306-70A>G NP_065068.1:n.1306-70A>G
XM_005245357.1:c.1306-70A>G XP_005245414.1:n.1306-70A>G
XM_011509804.1:c.1306-70A>G XP_011508106.1:n.1306-70A>G
NM_020335.3:c.1306-70A>G MANE Select NP_065068.1:n.1306-70A>G
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