Canonical Allele Identifier: CA988450683

Gene: HRH4

Linked Data

• dbSNP Id: rs1909607498
• gnomAD v3: 18-24460650-A-G
• gnomAD v4: 18-24460650-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460650A>G , CM000680.2:g.24460650A>G	GRCh38
NC_000018.9:g.22040614A>G , CM000680.1:g.22040614A>G	GRCh37
NC_000018.8:g.20294612A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.-79A>G MANE Select	ENSP00000256906.4:n.-79A>G
ENST00000256906.4:c.-79A>G	ENSP00000256906.4:n.-79A>G
NM_001143828.1:c.-79A>G	NP_001137300.1:n.-79A>G
NM_001160166.1:c.-79A>G	NP_001153638.1:n.-79A>G
NM_021624.3:c.-79A>G	NP_067637.2:n.-79A>G
XM_011526133.1:c.-79A>G	XP_011524435.1:n.-79A>G
XM_011526134.1:c.-79A>G	XP_011524436.1:n.-79A>G
NM_021624.4:c.-79A>G MANE Select	NP_067637.2:n.-79A>G
NM_001143828.2:c.-79A>G	NP_001137300.1:n.-79A>G
NM_001160166.2:c.-79A>G	NP_001153638.1:n.-79A>G