Canonical Allele Identifier: CA1009705807

Gene: LHX4

Linked Data

• gnomAD v3: 1-180266299-T-G
• gnomAD v4: 1-180266299-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266299T>G , CM000663.2:g.180266299T>G	GRCh38
NC_000001.10:g.180235434T>G , CM000663.1:g.180235434T>G	GRCh37
NC_000001.9:g.178502057T>G	NCBI36
NG_008081.1:g.40993T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263726.4:c.249-93T>G MANE Select	ENSP00000263726.2:n.249-93T>G
ENST00000263726.3:c.249-93T>G	ENSP00000263726.2:n.249-93T>G
ENST00000561113.1:c.186-93T>G
NM_033343.3:c.249-93T>G	NP_203129.1:n.249-93T>G
XM_011510105.1:c.66-93T>G	XP_011508407.1:n.66-93T>G
XM_011510106.1:c.66-93T>G	XP_011508408.1:n.66-93T>G
XM_011510107.1:c.23+46T>G	XP_011508409.1:n.23+46T>G
XM_011510108.1:c.23+46T>G	XP_011508410.1:n.23+46T>G
XM_011510105.2:c.66-93T>G	XP_011508407.1:n.66-93T>G
XM_011510106.3:c.66-93T>G	XP_011508408.1:n.66-93T>G
XM_011510108.2:c.23+46T>G	XP_011508410.1:n.23+46T>G
XM_017002755.1:c.23+46T>G	XP_016858244.1:n.23+46T>G
NM_033343.4:c.249-93T>G MANE Select	NP_203129.1:n.249-93T>G