Canonical Allele Identifier: CA402083722

Gene: HRH4

Linked Data

• gnomAD v4: 18-24477286-G-C
• MyVariant Identifiers: chr18:g.22057250G>C (hg19) ; chr18:g.24477286G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477286G>C , CM000680.2:g.24477286G>C	GRCh38
NC_000018.9:g.22057250G>C , CM000680.1:g.22057250G>C	GRCh37
NC_000018.8:g.20311248G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.897G>C MANE Select	ENSP00000256906.4:p.Arg299Ser
ENST00000256906.4:c.897G>C	ENSP00000256906.4:p.Arg299Ser
ENST00000426880.2:c.633G>C	ENSP00000402526.2:p.Arg211Ser
NM_001143828.1:c.633G>C	NP_001137300.1:p.Arg211Ser
NM_001160166.1:c.*529G>C	NP_001153638.1:n.*529G>C
NM_021624.3:c.897G>C	NP_067637.2:p.Arg299Ser
XM_011526133.1:c.357+8335G>C	XP_011524435.1:n.357+8335G>C
NM_021624.4:c.897G>C MANE Select	NP_067637.2:p.Arg299Ser
NM_001143828.2:c.633G>C	NP_001137300.1:p.Arg211Ser
NM_001160166.2:c.*529G>C	NP_001153638.1:n.*529G>C