Canonical Allele Identifier: CA31541285
Gene: VANGL2 HGNC NCBI

Linked Data

dbSNP Id: rs60322493
MyVariant Identifiers: chr1:g.160394836C>A (hg19) chr1:g.160425046C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425046C>A , CM000663.2:g.160425046C>A GRCh38
NC_000001.10:g.160394836C>A , CM000663.1:g.160394836C>A GRCh37
NC_000001.9:g.158661460C>A NCBI36
NG_023420.1:g.29473C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696602.1:c.1450-72C>A ENSP00000512747.1:n.1450-72C>A
ENST00000368061.3:c.1306-72C>A MANE Select ENSP00000357040.2:n.1306-72C>A
ENST00000368061.2:c.1306-72C>A ENSP00000357040.2:n.1306-72C>A
NM_020335.2:c.1306-72C>A NP_065068.1:n.1306-72C>A
XM_005245357.1:c.1306-72C>A XP_005245414.1:n.1306-72C>A
XM_011509804.1:c.1306-72C>A XP_011508106.1:n.1306-72C>A
NM_020335.3:c.1306-72C>A MANE Select NP_065068.1:n.1306-72C>A
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