Canonical Allele Identifier: CA297155740

Gene: HRH4

Linked Data

• dbSNP Id: rs894564616
• gnomAD v3: 18-24476769-C-G
• gnomAD v4: 18-24476769-C-G
• MyVariant Identifiers: chr18:g.22056733C>G (hg19) ; chr18:g.24476769C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476769C>G , CM000680.2:g.24476769C>G	GRCh38
NC_000018.9:g.22056733C>G , CM000680.1:g.22056733C>G	GRCh37
NC_000018.8:g.20310731C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.380C>G MANE Select	ENSP00000256906.4:p.Thr127Ser
ENST00000256906.4:c.380C>G	ENSP00000256906.4:p.Thr127Ser
ENST00000426880.2:c.194-78C>G	ENSP00000402526.2:n.194-78C>G
NM_001143828.1:c.194-78C>G	NP_001137300.1:n.194-78C>G
NM_001160166.1:c.*12C>G	NP_001153638.1:n.*12C>G
NM_021624.3:c.380C>G	NP_067637.2:p.Thr127Ser
XM_011526133.1:c.357+7818C>G	XP_011524435.1:n.357+7818C>G
NM_021624.4:c.380C>G MANE Select	NP_067637.2:p.Thr127Ser
NM_001143828.2:c.194-78C>G	NP_001137300.1:n.194-78C>G
NM_001160166.2:c.*12C>G	NP_001153638.1:n.*12C>G