Canonical Allele Identifier: CA402083782

Gene: HRH4

Linked Data

• dbSNP Id: rs1341014410
• MyVariant Identifiers: chr18:g.22057279T>C (hg19) ; chr18:g.24477315T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477315T>C , CM000680.2:g.24477315T>C	GRCh38
NC_000018.9:g.22057279T>C , CM000680.1:g.22057279T>C	GRCh37
NC_000018.8:g.20311277T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.926T>C MANE Select	ENSP00000256906.4:p.Leu309Ser
ENST00000256906.4:c.926T>C	ENSP00000256906.4:p.Leu309Ser
ENST00000426880.2:c.662T>C	ENSP00000402526.2:p.Leu221Ser
NM_001143828.1:c.662T>C	NP_001137300.1:p.Leu221Ser
NM_001160166.1:c.*558T>C	NP_001153638.1:n.*558T>C
NM_021624.3:c.926T>C	NP_067637.2:p.Leu309Ser
XM_011526133.1:c.357+8364T>C	XP_011524435.1:n.357+8364T>C
NM_021624.4:c.926T>C MANE Select	NP_067637.2:p.Leu309Ser
NM_001143828.2:c.662T>C	NP_001137300.1:p.Leu221Ser
NM_001160166.2:c.*558T>C	NP_001153638.1:n.*558T>C