Canonical Allele Identifier: CA250568
Gene: LHX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 9022
ClinVar RCV Id: RCV000009588
dbSNP Id: rs587776711

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136199660_136199682del , CM000671.2:g.136199660_136199682del GRCh38
NC_000009.11:g.139091506_139091528del , CM000671.1:g.139091506_139091528del GRCh37
NC_000009.10:g.138231327_138231349del NCBI36
NG_008097.1:g.10430_10452del

Transcript Alleles

HGVS Amino-acid change
ENST00000371746.9:c.467_469+20del
ENST00000371748.10:c.452_454+20del
ENST00000645419.1:n.1277_1279+20del
ENST00000371746.7:c.467_469+20del
ENST00000371748.9:c.452_454+20del
ENST00000619587.1:c.419_421+20del
NM_014564.3:c.467_469+20del
NM_178138.4:c.452_454+20del
XM_005263410.1:c.419_421+20del
NM_001363746.1:c.419_421+20del
NM_014564.4:c.467_469+20del
NM_178138.5:c.452_454+20del
XM_017015168.1:c.380_382+20del
NM_178138.6:c.452_454+20del
NM_014564.5:c.467_469+20del