Canonical Allele Identifier: CA503523538

Gene: HRH4

Linked Data

• dbSNP Id: rs1433609880
• gnomAD v2: 18-22056908-C-T
• gnomAD v4: 18-24476944-C-T
• MyVariant Identifiers: chr18:g.22056908C>T (hg19) ; chr18:g.24476944C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476944C>T , CM000680.2:g.24476944C>T	GRCh38
NC_000018.9:g.22056908C>T , CM000680.1:g.22056908C>T	GRCh37
NC_000018.8:g.20310906C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.555C>T MANE Select	ENSP00000256906.4:p.Ile185=
ENST00000256906.4:c.555C>T	ENSP00000256906.4:p.Ile185=
ENST00000426880.2:c.291C>T	ENSP00000402526.2:p.Ile97=
NM_001143828.1:c.291C>T	NP_001137300.1:p.Ile97=
NM_001160166.1:c.*187C>T	NP_001153638.1:n.*187C>T
NM_021624.3:c.555C>T	NP_067637.2:p.Ile185=
XM_011526133.1:c.357+7993C>T	XP_011524435.1:n.357+7993C>T
NM_021624.4:c.555C>T MANE Select	NP_067637.2:p.Ile185=
NM_001143828.2:c.291C>T	NP_001137300.1:p.Ile97=
NM_001160166.2:c.*187C>T	NP_001153638.1:n.*187C>T