Canonical Allele Identifier: CA2576475258

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460653T>C , CM000680.2:g.24460653T>C	GRCh38
NC_000018.9:g.22040617T>C , CM000680.1:g.22040617T>C	GRCh37
NC_000018.8:g.20294615T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.-76T>C MANE Select	ENSP00000256906.4:n.-76T>C
ENST00000256906.4:c.-76T>C	ENSP00000256906.4:n.-76T>C
NM_001143828.1:c.-76T>C	NP_001137300.1:n.-76T>C
NM_001160166.1:c.-76T>C	NP_001153638.1:n.-76T>C
NM_021624.3:c.-76T>C	NP_067637.2:n.-76T>C
XM_011526133.1:c.-76T>C	XP_011524435.1:n.-76T>C
XM_011526134.1:c.-76T>C	XP_011524436.1:n.-76T>C
NM_021624.4:c.-76T>C MANE Select	NP_067637.2:n.-76T>C
NM_001143828.2:c.-76T>C	NP_001137300.1:n.-76T>C
NM_001160166.2:c.-76T>C	NP_001153638.1:n.-76T>C