Canonical Allele Identifier: CA1345569660

Gene: HRH1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11191093G= , CM000665.2:g.11191093G=	GRCh38
NC_000003.11:g.11232779G= , CM000665.1:g.11232779G=	GRCh37
NC_000003.10:g.11207779G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431010.3:c.-36+36539G= MANE Select	ENSP00000397028.2:n.-36+36539G=
ENST00000431010.2:c.-36+36539G=	ENSP00000397028.2:n.-36+36539G=
ENST00000438284.2:c.-36+53694G=	ENSP00000406705.2:n.-36+53694G=
NM_001098212.1:c.-36+36539G=	NP_001091682.1:n.-36+36539G=
NM_001098213.1:c.-36+53694G=	NP_001091683.1:n.-36+53694G=
XM_011533653.1:c.-36+35962G=	XP_011531955.1:n.-36+35962G=
XM_011533653.2:c.-36+35962G=	XP_011531955.1:n.-36+35962G=
XM_017006284.1:c.-36+35204G=	XP_016861773.1:n.-36+35204G=
NM_001098212.2:c.-36+36539G= MANE Select	NP_001091682.1:n.-36+36539G=
NM_001098213.2:c.-36+53694G=	NP_001091683.1:n.-36+53694G=