Canonical Allele Identifier: CA297155664

Gene: HRH4

Linked Data

• dbSNP Id: rs1049369402
• gnomAD v3: 18-24476581-C-A
• gnomAD v4: 18-24476581-C-A
• MyVariant Identifiers: chr18:g.22056545C>A (hg19) ; chr18:g.24476581C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476581C>A , CM000680.2:g.24476581C>A	GRCh38
NC_000018.9:g.22056545C>A , CM000680.1:g.22056545C>A	GRCh37
NC_000018.8:g.20310543C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.358-166C>A MANE Select	ENSP00000256906.4:n.358-166C>A
ENST00000256906.4:c.358-166C>A	ENSP00000256906.4:n.358-166C>A
ENST00000426880.2:c.194-266C>A	ENSP00000402526.2:n.194-266C>A
NM_001143828.1:c.194-266C>A	NP_001137300.1:n.194-266C>A
NM_001160166.1:c.194-166C>A	NP_001153638.1:n.194-166C>A
NM_021624.3:c.358-166C>A	NP_067637.2:n.358-166C>A
XM_011526133.1:c.357+7630C>A	XP_011524435.1:n.357+7630C>A
NM_021624.4:c.358-166C>A MANE Select	NP_067637.2:n.358-166C>A
NM_001143828.2:c.194-266C>A	NP_001137300.1:n.194-266C>A
NM_001160166.2:c.194-166C>A	NP_001153638.1:n.194-166C>A