Canonical Allele Identifier: CA402083160

Gene: HRH4

Linked Data

• gnomAD v4: 18-24477024-G-C
• MyVariant Identifiers: chr18:g.22056988G>C (hg19) ; chr18:g.24477024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477024G>C , CM000680.2:g.24477024G>C	GRCh38
NC_000018.9:g.22056988G>C , CM000680.1:g.22056988G>C	GRCh37
NC_000018.8:g.20310986G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.635G>C MANE Select	ENSP00000256906.4:p.Ser212Thr
ENST00000256906.4:c.635G>C	ENSP00000256906.4:p.Ser212Thr
ENST00000426880.2:c.371G>C	ENSP00000402526.2:p.Ser124Thr
NM_001143828.1:c.371G>C	NP_001137300.1:p.Ser124Thr
NM_001160166.1:c.*267G>C	NP_001153638.1:n.*267G>C
NM_021624.3:c.635G>C	NP_067637.2:p.Ser212Thr
XM_011526133.1:c.357+8073G>C	XP_011524435.1:n.357+8073G>C
NM_021624.4:c.635G>C MANE Select	NP_067637.2:p.Ser212Thr
NM_001143828.2:c.371G>C	NP_001137300.1:p.Ser124Thr
NM_001160166.2:c.*267G>C	NP_001153638.1:n.*267G>C