Canonical Allele Identifier: CA2648683995
Gene: VANGL2 HGNC NCBI

Linked Data

gnomAD v4: 1-160425038-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425038T>G , CM000663.2:g.160425038T>G GRCh38
NC_000001.10:g.160394828T>G , CM000663.1:g.160394828T>G GRCh37
NC_000001.9:g.158661452T>G NCBI36
NG_023420.1:g.29465T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696602.1:c.1450-80T>G ENSP00000512747.1:n.1450-80T>G
ENST00000368061.3:c.1306-80T>G MANE Select ENSP00000357040.2:n.1306-80T>G
ENST00000368061.2:c.1306-80T>G ENSP00000357040.2:n.1306-80T>G
NM_020335.2:c.1306-80T>G NP_065068.1:n.1306-80T>G
XM_005245357.1:c.1306-80T>G XP_005245414.1:n.1306-80T>G
XM_011509804.1:c.1306-80T>G XP_011508106.1:n.1306-80T>G
NM_020335.3:c.1306-80T>G MANE Select NP_065068.1:n.1306-80T>G
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