Canonical Allele Identifier: CA1210607026

Gene: LHX4

Linked Data

• dbSNP Id: rs1571282900
• gnomAD v4: 1-180266307-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266307T>G , CM000663.2:g.180266307T>G	GRCh38
NC_000001.10:g.180235442T>G , CM000663.1:g.180235442T>G	GRCh37
NC_000001.9:g.178502065T>G	NCBI36
NG_008081.1:g.41001T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263726.4:c.249-85T>G MANE Select	ENSP00000263726.2:n.249-85T>G
ENST00000263726.3:c.249-85T>G	ENSP00000263726.2:n.249-85T>G
ENST00000561113.1:c.186-85T>G
NM_033343.3:c.249-85T>G	NP_203129.1:n.249-85T>G
XM_011510105.1:c.66-85T>G	XP_011508407.1:n.66-85T>G
XM_011510106.1:c.66-85T>G	XP_011508408.1:n.66-85T>G
XM_011510107.1:c.23+54T>G	XP_011508409.1:n.23+54T>G
XM_011510108.1:c.23+54T>G	XP_011508410.1:n.23+54T>G
XM_011510105.2:c.66-85T>G	XP_011508407.1:n.66-85T>G
XM_011510106.3:c.66-85T>G	XP_011508408.1:n.66-85T>G
XM_011510108.2:c.23+54T>G	XP_011508410.1:n.23+54T>G
XM_017002755.1:c.23+54T>G	XP_016858244.1:n.23+54T>G
NM_033343.4:c.249-85T>G MANE Select	NP_203129.1:n.249-85T>G