Canonical Allele Identifier: CA402082896

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22056871A>C (hg19) ; chr18:g.24476907A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476907A>C , CM000680.2:g.24476907A>C	GRCh38
NC_000018.9:g.22056871A>C , CM000680.1:g.22056871A>C	GRCh37
NC_000018.8:g.20310869A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.518A>C MANE Select	ENSP00000256906.4:p.Tyr173Ser
ENST00000256906.4:c.518A>C	ENSP00000256906.4:p.Tyr173Ser
ENST00000426880.2:c.254A>C	ENSP00000402526.2:p.Tyr85Ser
NM_001143828.1:c.254A>C	NP_001137300.1:p.Tyr85Ser
NM_001160166.1:c.*150A>C	NP_001153638.1:n.*150A>C
NM_021624.3:c.518A>C	NP_067637.2:p.Tyr173Ser
XM_011526133.1:c.357+7956A>C	XP_011524435.1:n.357+7956A>C
NM_021624.4:c.518A>C MANE Select	NP_067637.2:p.Tyr173Ser
NM_001143828.2:c.254A>C	NP_001137300.1:p.Tyr85Ser
NM_001160166.2:c.*150A>C	NP_001153638.1:n.*150A>C