Canonical Allele Identifier: CA2641326640
Gene: HRH4 HGNC NCBI

Linked Data

gnomAD v4: 18-24476642-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476642T>A , CM000680.2:g.24476642T>A GRCh38
NC_000018.9:g.22056606T>A , CM000680.1:g.22056606T>A GRCh37
NC_000018.8:g.20310604T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.358-105T>A MANE Select ENSP00000256906.4:n.358-105T>A
ENST00000256906.4:c.358-105T>A ENSP00000256906.4:n.358-105T>A
ENST00000426880.2:c.194-205T>A ENSP00000402526.2:n.194-205T>A
NM_001143828.1:c.194-205T>A NP_001137300.1:n.194-205T>A
NM_001160166.1:c.194-105T>A NP_001153638.1:n.194-105T>A
NM_021624.3:c.358-105T>A NP_067637.2:n.358-105T>A
XM_011526133.1:c.357+7691T>A XP_011524435.1:n.357+7691T>A
NM_021624.4:c.358-105T>A MANE Select NP_067637.2:n.358-105T>A
NM_001143828.2:c.194-205T>A NP_001137300.1:n.194-205T>A
NM_001160166.2:c.194-105T>A NP_001153638.1:n.194-105T>A
Search 100 bp 5'
Search 100 bp 3'