Canonical Allele Identifier: CA1202313698
Gene: VANGL2 HGNC NCBI

Linked Data

dbSNP Id: rs1651402850
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425061T>C , CM000663.2:g.160425061T>C GRCh38
NC_000001.10:g.160394851T>C , CM000663.1:g.160394851T>C GRCh37
NC_000001.9:g.158661475T>C NCBI36
NG_023420.1:g.29488T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-57T>C ENSP00000512747.1:n.1450-57T>C
ENST00000368061.3:c.1306-57T>C MANE Select ENSP00000357040.2:n.1306-57T>C
ENST00000368061.2:c.1306-57T>C ENSP00000357040.2:n.1306-57T>C
NM_020335.2:c.1306-57T>C NP_065068.1:n.1306-57T>C
XM_005245357.1:c.1306-57T>C XP_005245414.1:n.1306-57T>C
XM_011509804.1:c.1306-57T>C XP_011508106.1:n.1306-57T>C
NM_020335.3:c.1306-57T>C MANE Select NP_065068.1:n.1306-57T>C
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