Canonical Allele Identifier: CA8919889

Gene: HRH4

Linked Data

• dbSNP Id: rs58154316
• ExAC: 18:22057204 C / G
• gnomAD v2: 18-22057204-C-G
• gnomAD v3: 18-24477240-C-G
• gnomAD v4: 18-24477240-C-G
• MyVariant Identifiers: chr18:g.22057204C>G (hg19) ; chr18:g.24477240C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477240C>G , CM000680.2:g.24477240C>G	GRCh38
NC_000018.9:g.22057204C>G , CM000680.1:g.22057204C>G	GRCh37
NC_000018.8:g.20311202C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.851C>G MANE Select	ENSP00000256906.4:p.Ser284Cys
ENST00000256906.4:c.851C>G	ENSP00000256906.4:p.Ser284Cys
ENST00000426880.2:c.587C>G	ENSP00000402526.2:p.Ser196Cys
NM_001143828.1:c.587C>G	NP_001137300.1:p.Ser196Cys
NM_001160166.1:c.*483C>G	NP_001153638.1:n.*483C>G
NM_021624.3:c.851C>G	NP_067637.2:p.Ser284Cys
XM_011526133.1:c.357+8289C>G	XP_011524435.1:n.357+8289C>G
NM_021624.4:c.851C>G MANE Select	NP_067637.2:p.Ser284Cys
NM_001143828.2:c.587C>G	NP_001137300.1:p.Ser196Cys
NM_001160166.2:c.*483C>G	NP_001153638.1:n.*483C>G