Canonical Allele Identifier: CA2641326609

Gene: HRH4

Linked Data

• gnomAD v4: 18-24476626-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476626T>A , CM000680.2:g.24476626T>A	GRCh38
NC_000018.9:g.22056590T>A , CM000680.1:g.22056590T>A	GRCh37
NC_000018.8:g.20310588T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.358-121T>A MANE Select	ENSP00000256906.4:n.358-121T>A
ENST00000256906.4:c.358-121T>A	ENSP00000256906.4:n.358-121T>A
ENST00000426880.2:c.194-221T>A	ENSP00000402526.2:n.194-221T>A
NM_001143828.1:c.194-221T>A	NP_001137300.1:n.194-221T>A
NM_001160166.1:c.194-121T>A	NP_001153638.1:n.194-121T>A
NM_021624.3:c.358-121T>A	NP_067637.2:n.358-121T>A
XM_011526133.1:c.357+7675T>A	XP_011524435.1:n.357+7675T>A
NM_021624.4:c.358-121T>A MANE Select	NP_067637.2:n.358-121T>A
NM_001143828.2:c.194-221T>A	NP_001137300.1:n.194-221T>A
NM_001160166.2:c.194-121T>A	NP_001153638.1:n.194-121T>A