Canonical Allele Identifier: CA2641325522

Gene: HRH4

Linked Data

• gnomAD v4: 18-24460640-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460640C>T , CM000680.2:g.24460640C>T	GRCh38
NC_000018.9:g.22040604C>T , CM000680.1:g.22040604C>T	GRCh37
NC_000018.8:g.20294602C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.-89C>T MANE Select	ENSP00000256906.4:n.-89C>T
ENST00000256906.4:c.-89C>T	ENSP00000256906.4:n.-89C>T
NM_001143828.1:c.-89C>T	NP_001137300.1:n.-89C>T
NM_001160166.1:c.-89C>T	NP_001153638.1:n.-89C>T
NM_021624.3:c.-89C>T	NP_067637.2:n.-89C>T
XM_011526133.1:c.-89C>T	XP_011524435.1:n.-89C>T
XM_011526134.1:c.-89C>T	XP_011524436.1:n.-89C>T
NM_021624.4:c.-89C>T MANE Select	NP_067637.2:n.-89C>T
NM_001143828.2:c.-89C>T	NP_001137300.1:n.-89C>T
NM_001160166.2:c.-89C>T	NP_001153638.1:n.-89C>T