Canonical Allele Identifier: CA2648683997
Gene: VANGL2 HGNC NCBI

Linked Data

gnomAD v4: 1-160425044-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425044A>C , CM000663.2:g.160425044A>C GRCh38
NC_000001.10:g.160394834A>C , CM000663.1:g.160394834A>C GRCh37
NC_000001.9:g.158661458A>C NCBI36
NG_023420.1:g.29471A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696602.1:c.1450-74A>C ENSP00000512747.1:n.1450-74A>C
ENST00000368061.3:c.1306-74A>C MANE Select ENSP00000357040.2:n.1306-74A>C
ENST00000368061.2:c.1306-74A>C ENSP00000357040.2:n.1306-74A>C
NM_020335.2:c.1306-74A>C NP_065068.1:n.1306-74A>C
XM_005245357.1:c.1306-74A>C XP_005245414.1:n.1306-74A>C
XM_011509804.1:c.1306-74A>C XP_011508106.1:n.1306-74A>C
NM_020335.3:c.1306-74A>C MANE Select NP_065068.1:n.1306-74A>C
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