Canonical Allele Identifier: CA11350995

Gene: HRH1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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