Canonical Allele Identifier: CA527214774

Gene: LHX4

Linked Data

• dbSNP Id: rs1423274091
• gnomAD v2: 1-180235429-C-T
• gnomAD v3: 1-180266294-C-T
• gnomAD v4: 1-180266294-C-T
• MyVariant Identifiers: chr1:g.180235429C>T (hg19) ; chr1:g.180266294C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266294C>T , CM000663.2:g.180266294C>T	GRCh38
NC_000001.10:g.180235429C>T , CM000663.1:g.180235429C>T	GRCh37
NC_000001.9:g.178502052C>T	NCBI36
NG_008081.1:g.40988C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263726.4:c.249-98C>T MANE Select	ENSP00000263726.2:n.249-98C>T
ENST00000263726.3:c.249-98C>T	ENSP00000263726.2:n.249-98C>T
ENST00000561113.1:c.186-98C>T
NM_033343.3:c.249-98C>T	NP_203129.1:n.249-98C>T
XM_011510105.1:c.66-98C>T	XP_011508407.1:n.66-98C>T
XM_011510106.1:c.66-98C>T	XP_011508408.1:n.66-98C>T
XM_011510107.1:c.23+41C>T	XP_011508409.1:n.23+41C>T
XM_011510108.1:c.23+41C>T	XP_011508410.1:n.23+41C>T
XM_011510105.2:c.66-98C>T	XP_011508407.1:n.66-98C>T
XM_011510106.3:c.66-98C>T	XP_011508408.1:n.66-98C>T
XM_011510108.2:c.23+41C>T	XP_011508410.1:n.23+41C>T
XM_017002755.1:c.23+41C>T	XP_016858244.1:n.23+41C>T
NM_033343.4:c.249-98C>T MANE Select	NP_203129.1:n.249-98C>T