Canonical Allele Identifier: CA2290570380

Gene: HRH4

Linked Data

• dbSNP Id: rs1909607138
• gnomAD v4: 18-24460643-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460643T>G , CM000680.2:g.24460643T>G	GRCh38
NC_000018.9:g.22040607T>G , CM000680.1:g.22040607T>G	GRCh37
NC_000018.8:g.20294605T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.-86T>G MANE Select	ENSP00000256906.4:n.-86T>G
ENST00000256906.4:c.-86T>G	ENSP00000256906.4:n.-86T>G
NM_001143828.1:c.-86T>G	NP_001137300.1:n.-86T>G
NM_001160166.1:c.-86T>G	NP_001153638.1:n.-86T>G
NM_021624.3:c.-86T>G	NP_067637.2:n.-86T>G
XM_011526133.1:c.-86T>G	XP_011524435.1:n.-86T>G
XM_011526134.1:c.-86T>G	XP_011524436.1:n.-86T>G
NM_021624.4:c.-86T>G MANE Select	NP_067637.2:n.-86T>G
NM_001143828.2:c.-86T>G	NP_001137300.1:n.-86T>G
NM_001160166.2:c.-86T>G	NP_001153638.1:n.-86T>G