Canonical Allele Identifier: CA988425700

Gene: HRH4

Linked Data

• dbSNP Id: rs1909877634
• gnomAD v3: 18-24469539-A-C
• gnomAD v4: 18-24469539-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24469539A>C , CM000680.2:g.24469539A>C	GRCh38
NC_000018.9:g.22049503A>C , CM000680.1:g.22049503A>C	GRCh37
NC_000018.8:g.20303501A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.357+588A>C MANE Select	ENSP00000256906.4:n.357+588A>C
ENST00000256906.4:c.357+588A>C	ENSP00000256906.4:n.357+588A>C
ENST00000426880.2:c.194-7308A>C	ENSP00000402526.2:n.194-7308A>C
NM_001143828.1:c.194-7308A>C	NP_001137300.1:n.194-7308A>C
NM_001160166.1:c.194-7208A>C	NP_001153638.1:n.194-7208A>C
NM_021624.3:c.357+588A>C	NP_067637.2:n.357+588A>C
XM_011526133.1:c.357+588A>C	XP_011524435.1:n.357+588A>C
XM_011526134.1:c.357+588A>C	XP_011524436.1:n.357+588A>C
NM_021624.4:c.357+588A>C MANE Select	NP_067637.2:n.357+588A>C
NM_001143828.2:c.194-7308A>C	NP_001137300.1:n.194-7308A>C
NM_001160166.2:c.194-7208A>C	NP_001153638.1:n.194-7208A>C