Canonical Allele Identifier: CA402082900

Gene: HRH4

Linked Data

• gnomAD v4: 18-24476908-C-G
• MyVariant Identifiers: chr18:g.22056872C>G (hg19) ; chr18:g.24476908C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476908C>G , CM000680.2:g.24476908C>G	GRCh38
NC_000018.9:g.22056872C>G , CM000680.1:g.22056872C>G	GRCh37
NC_000018.8:g.20310870C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.519C>G MANE Select	ENSP00000256906.4:p.Tyr173Ter
ENST00000256906.4:c.519C>G	ENSP00000256906.4:p.Tyr173Ter
ENST00000426880.2:c.255C>G	ENSP00000402526.2:p.Tyr85Ter
NM_001143828.1:c.255C>G	NP_001137300.1:p.Tyr85Ter
NM_001160166.1:c.*151C>G	NP_001153638.1:n.*151C>G
NM_021624.3:c.519C>G	NP_067637.2:p.Tyr173Ter
XM_011526133.1:c.357+7957C>G	XP_011524435.1:n.357+7957C>G
NM_021624.4:c.519C>G MANE Select	NP_067637.2:p.Tyr173Ter
NM_001143828.2:c.255C>G	NP_001137300.1:p.Tyr85Ter
NM_001160166.2:c.*151C>G	NP_001153638.1:n.*151C>G