Canonical Allele Identifier: CA2290574160

Gene: HRH4

Linked Data

• dbSNP Id: rs1909877771

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24469545T>C , CM000680.2:g.24469545T>C	GRCh38
NC_000018.9:g.22049509T>C , CM000680.1:g.22049509T>C	GRCh37
NC_000018.8:g.20303507T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.357+594T>C MANE Select	ENSP00000256906.4:n.357+594T>C
ENST00000256906.4:c.357+594T>C	ENSP00000256906.4:n.357+594T>C
ENST00000426880.2:c.194-7302T>C	ENSP00000402526.2:n.194-7302T>C
NM_001143828.1:c.194-7302T>C	NP_001137300.1:n.194-7302T>C
NM_001160166.1:c.194-7202T>C	NP_001153638.1:n.194-7202T>C
NM_021624.3:c.357+594T>C	NP_067637.2:n.357+594T>C
XM_011526133.1:c.357+594T>C	XP_011524435.1:n.357+594T>C
XM_011526134.1:c.357+594T>C	XP_011524436.1:n.357+594T>C
NM_021624.4:c.357+594T>C MANE Select	NP_067637.2:n.357+594T>C
NM_001143828.2:c.194-7302T>C	NP_001137300.1:n.194-7302T>C
NM_001160166.2:c.194-7202T>C	NP_001153638.1:n.194-7202T>C