Canonical Allele Identifier: CA1009705810

Gene: LHX4

Linked Data

• dbSNP Id: rs1648309514
• gnomAD v3: 1-180266305-G-C
• gnomAD v4: 1-180266305-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266305G>C , CM000663.2:g.180266305G>C	GRCh38
NC_000001.10:g.180235440G>C , CM000663.1:g.180235440G>C	GRCh37
NC_000001.9:g.178502063G>C	NCBI36
NG_008081.1:g.40999G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263726.4:c.249-87G>C MANE Select	ENSP00000263726.2:n.249-87G>C
ENST00000263726.3:c.249-87G>C	ENSP00000263726.2:n.249-87G>C
ENST00000561113.1:c.186-87G>C
NM_033343.3:c.249-87G>C	NP_203129.1:n.249-87G>C
XM_011510105.1:c.66-87G>C	XP_011508407.1:n.66-87G>C
XM_011510106.1:c.66-87G>C	XP_011508408.1:n.66-87G>C
XM_011510107.1:c.23+52G>C	XP_011508409.1:n.23+52G>C
XM_011510108.1:c.23+52G>C	XP_011508410.1:n.23+52G>C
XM_011510105.2:c.66-87G>C	XP_011508407.1:n.66-87G>C
XM_011510106.3:c.66-87G>C	XP_011508408.1:n.66-87G>C
XM_011510108.2:c.23+52G>C	XP_011508410.1:n.23+52G>C
XM_017002755.1:c.23+52G>C	XP_016858244.1:n.23+52G>C
NM_033343.4:c.249-87G>C MANE Select	NP_203129.1:n.249-87G>C