Canonical Allele Identifier: CA777784926

Gene: HRH4

Linked Data

• dbSNP Id: rs1280031360
• gnomAD v3: 18-24460652-G-A
• gnomAD v4: 18-24460652-G-A
• MyVariant Identifiers: chr18:g.22040616G>A (hg19) ; chr18:g.24460652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460652G>A , CM000680.2:g.24460652G>A	GRCh38
NC_000018.9:g.22040616G>A , CM000680.1:g.22040616G>A	GRCh37
NC_000018.8:g.20294614G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.-77G>A MANE Select	ENSP00000256906.4:n.-77G>A
ENST00000256906.4:c.-77G>A	ENSP00000256906.4:n.-77G>A
NM_001143828.1:c.-77G>A	NP_001137300.1:n.-77G>A
NM_001160166.1:c.-77G>A	NP_001153638.1:n.-77G>A
NM_021624.3:c.-77G>A	NP_067637.2:n.-77G>A
XM_011526133.1:c.-77G>A	XP_011524435.1:n.-77G>A
XM_011526134.1:c.-77G>A	XP_011524436.1:n.-77G>A
NM_021624.4:c.-77G>A MANE Select	NP_067637.2:n.-77G>A
NM_001143828.2:c.-77G>A	NP_001137300.1:n.-77G>A
NM_001160166.2:c.-77G>A	NP_001153638.1:n.-77G>A