Canonical Allele Identifier: CA1345569661
Gene: HRH1 HGNC NCBI

Linked Data

dbSNP Id: rs4684059
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Genomic Alleles

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

Transcript Alleles

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