Canonical Allele Identifier: CA1202313688
Gene: VANGL2 HGNC NCBI

Linked Data

dbSNP Id: rs1651402385
gnomAD v4: 1-160425035-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425035G>T , CM000663.2:g.160425035G>T GRCh38
NC_000001.10:g.160394825G>T , CM000663.1:g.160394825G>T GRCh37
NC_000001.9:g.158661449G>T NCBI36
NG_023420.1:g.29462G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-83G>T ENSP00000512747.1:n.1450-83G>T
ENST00000368061.3:c.1306-83G>T MANE Select ENSP00000357040.2:n.1306-83G>T
ENST00000368061.2:c.1306-83G>T ENSP00000357040.2:n.1306-83G>T
NM_020335.2:c.1306-83G>T NP_065068.1:n.1306-83G>T
XM_005245357.1:c.1306-83G>T XP_005245414.1:n.1306-83G>T
XM_011509804.1:c.1306-83G>T XP_011508106.1:n.1306-83G>T
NM_020335.3:c.1306-83G>T MANE Select NP_065068.1:n.1306-83G>T
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