Canonical Allele Identifier: CA1210606949

Gene: LHX4

Linked Data

• dbSNP Id: rs1648306006

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266200A>C , CM000663.2:g.180266200A>C	GRCh38
NC_000001.10:g.180235335A>C , CM000663.1:g.180235335A>C	GRCh37
NC_000001.9:g.178501958A>C	NCBI36
NG_008081.1:g.40894A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.249-192A>C MANE Select	ENSP00000263726.2:n.249-192A>C
ENST00000263726.3:c.249-192A>C	ENSP00000263726.2:n.249-192A>C
ENST00000561113.1:c.186-192A>C
NM_033343.3:c.249-192A>C	NP_203129.1:n.249-192A>C
XM_011510105.1:c.66-192A>C	XP_011508407.1:n.66-192A>C
XM_011510106.1:c.66-192A>C	XP_011508408.1:n.66-192A>C
XM_011510107.1:c.-28-3A>C	XP_011508409.1:n.-28-3A>C
XM_011510108.1:c.-28-3A>C	XP_011508410.1:n.-28-3A>C
XM_011510105.2:c.66-192A>C	XP_011508407.1:n.66-192A>C
XM_011510106.3:c.66-192A>C	XP_011508408.1:n.66-192A>C
XM_011510108.2:c.-28-3A>C	XP_011508410.1:n.-28-3A>C
XM_017002755.1:c.-31A>C	XP_016858244.1:n.-31A>C
NM_033343.4:c.249-192A>C MANE Select	NP_203129.1:n.249-192A>C