Canonical Allele Identifier: CA2290577467
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1174058865
gnomAD v4: 18-24476621-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476621C>A , CM000680.2:g.24476621C>A GRCh38
NC_000018.9:g.22056585C>A , CM000680.1:g.22056585C>A GRCh37
NC_000018.8:g.20310583C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.358-126C>A MANE Select ENSP00000256906.4:n.358-126C>A
ENST00000256906.4:c.358-126C>A ENSP00000256906.4:n.358-126C>A
ENST00000426880.2:c.194-226C>A ENSP00000402526.2:n.194-226C>A
NM_001143828.1:c.194-226C>A NP_001137300.1:n.194-226C>A
NM_001160166.1:c.194-126C>A NP_001153638.1:n.194-126C>A
NM_021624.3:c.358-126C>A NP_067637.2:n.358-126C>A
XM_011526133.1:c.357+7670C>A XP_011524435.1:n.357+7670C>A
NM_021624.4:c.358-126C>A MANE Select NP_067637.2:n.358-126C>A
NM_001143828.2:c.194-226C>A NP_001137300.1:n.194-226C>A
NM_001160166.2:c.194-126C>A NP_001153638.1:n.194-126C>A
Search 100 bp 5'
Search 100 bp 3'