Canonical Allele Identifier: CA1345595612

Gene: HRH1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11248436G= , CM000665.2:g.11248436G=	GRCh38
NC_000003.11:g.11290122G= , CM000665.1:g.11290122G=	GRCh37
NC_000003.10:g.11265122G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431010.3:c.-35-10567G= MANE Select	ENSP00000397028.2:n.-35-10567G=
ENST00000413416.1:c.-35-10567G=	ENSP00000392383.1:n.-35-10567G=
ENST00000431010.2:c.-35-10567G=	ENSP00000397028.2:n.-35-10567G=
ENST00000438284.2:c.-35-10567G=	ENSP00000406705.2:n.-35-10567G=
NM_001098211.1:c.-35-10567G=	NP_001091681.1:n.-35-10567G=
NM_001098212.1:c.-35-10567G=	NP_001091682.1:n.-35-10567G=
NM_001098213.1:c.-35-10567G=	NP_001091683.1:n.-35-10567G=
XM_011533652.1:c.-193-4261G=	XP_011531954.1:n.-193-4261G=
XM_011533653.1:c.-35-10567G=	XP_011531955.1:n.-35-10567G=
XM_011533654.1:c.-35-10567G=	XP_011531956.1:n.-35-10567G=
XM_011533653.2:c.-35-10567G=	XP_011531955.1:n.-35-10567G=
XM_017006284.1:c.-35-10567G=	XP_016861773.1:n.-35-10567G=
NM_001098211.2:c.-35-10567G=	NP_001091681.1:n.-35-10567G=
NM_001098212.2:c.-35-10567G= MANE Select	NP_001091682.1:n.-35-10567G=
NM_001098213.2:c.-35-10567G=	NP_001091683.1:n.-35-10567G=