Canonical Allele Identifier: CA402083258

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22057036T>C (hg19) ; chr18:g.24477072T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477072T>C , CM000680.2:g.24477072T>C	GRCh38
NC_000018.9:g.22057036T>C , CM000680.1:g.22057036T>C	GRCh37
NC_000018.8:g.20311034T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.683T>C MANE Select	ENSP00000256906.4:p.Phe228Ser
ENST00000256906.4:c.683T>C	ENSP00000256906.4:p.Phe228Ser
ENST00000426880.2:c.419T>C	ENSP00000402526.2:p.Phe140Ser
NM_001143828.1:c.419T>C	NP_001137300.1:p.Phe140Ser
NM_001160166.1:c.*315T>C	NP_001153638.1:n.*315T>C
NM_021624.3:c.683T>C	NP_067637.2:p.Phe228Ser
XM_011526133.1:c.357+8121T>C	XP_011524435.1:n.357+8121T>C
NM_021624.4:c.683T>C MANE Select	NP_067637.2:p.Phe228Ser
NM_001143828.2:c.419T>C	NP_001137300.1:p.Phe140Ser
NM_001160166.2:c.*315T>C	NP_001153638.1:n.*315T>C