Canonical Allele Identifier: CA628691040

Gene: HRH4

Linked Data

• dbSNP Id: rs1435452558
• gnomAD v2: 18-22049539-T-A
• gnomAD v3: 18-24469575-T-A
• gnomAD v4: 18-24469575-T-A
• MyVariant Identifiers: chr18:g.22049539T>A (hg19) ; chr18:g.24469575T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24469575T>A , CM000680.2:g.24469575T>A	GRCh38
NC_000018.9:g.22049539T>A , CM000680.1:g.22049539T>A	GRCh37
NC_000018.8:g.20303537T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.357+624T>A MANE Select	ENSP00000256906.4:n.357+624T>A
ENST00000256906.4:c.357+624T>A	ENSP00000256906.4:n.357+624T>A
ENST00000426880.2:c.194-7272T>A	ENSP00000402526.2:n.194-7272T>A
NM_001143828.1:c.194-7272T>A	NP_001137300.1:n.194-7272T>A
NM_001160166.1:c.194-7172T>A	NP_001153638.1:n.194-7172T>A
NM_021624.3:c.357+624T>A	NP_067637.2:n.357+624T>A
XM_011526133.1:c.357+624T>A	XP_011524435.1:n.357+624T>A
XM_011526134.1:c.357+624T>A	XP_011524436.1:n.357+624T>A
NM_021624.4:c.357+624T>A MANE Select	NP_067637.2:n.357+624T>A
NM_001143828.2:c.194-7272T>A	NP_001137300.1:n.194-7272T>A
NM_001160166.2:c.194-7172T>A	NP_001153638.1:n.194-7172T>A