Canonical Allele Identifier: CA402082772

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22056818G>C (hg19) ; chr18:g.24476854G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476854G>C , CM000680.2:g.24476854G>C	GRCh38
NC_000018.9:g.22056818G>C , CM000680.1:g.22056818G>C	GRCh37
NC_000018.8:g.20310816G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.465G>C MANE Select	ENSP00000256906.4:p.Glu155Asp
ENST00000256906.4:c.465G>C	ENSP00000256906.4:p.Glu155Asp
ENST00000426880.2:c.201G>C	ENSP00000402526.2:p.Glu67Asp
NM_001143828.1:c.201G>C	NP_001137300.1:p.Glu67Asp
NM_001160166.1:c.*97G>C	NP_001153638.1:n.*97G>C
NM_021624.3:c.465G>C	NP_067637.2:p.Glu155Asp
XM_011526133.1:c.357+7903G>C	XP_011524435.1:n.357+7903G>C
NM_021624.4:c.465G>C MANE Select	NP_067637.2:p.Glu155Asp
NM_001143828.2:c.201G>C	NP_001137300.1:p.Glu67Asp
NM_001160166.2:c.*97G>C	NP_001153638.1:n.*97G>C