Canonical Allele Identifier: CA2290570382
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1909607224
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460645T>C , CM000680.2:g.24460645T>C GRCh38
NC_000018.9:g.22040609T>C , CM000680.1:g.22040609T>C GRCh37
NC_000018.8:g.20294607T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.-84T>C MANE Select ENSP00000256906.4:n.-84T>C
ENST00000256906.4:c.-84T>C ENSP00000256906.4:n.-84T>C
NM_001143828.1:c.-84T>C NP_001137300.1:n.-84T>C
NM_001160166.1:c.-84T>C NP_001153638.1:n.-84T>C
NM_021624.3:c.-84T>C NP_067637.2:n.-84T>C
XM_011526133.1:c.-84T>C XP_011524435.1:n.-84T>C
XM_011526134.1:c.-84T>C XP_011524436.1:n.-84T>C
NM_021624.4:c.-84T>C MANE Select NP_067637.2:n.-84T>C
NM_001143828.2:c.-84T>C NP_001137300.1:n.-84T>C
NM_001160166.2:c.-84T>C NP_001153638.1:n.-84T>C
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