Canonical Allele Identifier: CA503522998

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22056716T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476752T>C , CM000680.2:g.24476752T>C	GRCh38
NC_000018.9:g.22056716T>C , CM000680.1:g.22056716T>C	GRCh37
NC_000018.8:g.20310714T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.363T>C MANE Select	ENSP00000256906.4:p.Ser121=
ENST00000256906.4:c.363T>C	ENSP00000256906.4:p.Ser121=
ENST00000426880.2:c.194-95T>C	ENSP00000402526.2:n.194-95T>C
NM_001143828.1:c.194-95T>C	NP_001137300.1:n.194-95T>C
NM_001160166.1:c.199T>C	NP_001153638.1:p.Leu67=
NM_021624.3:c.363T>C	NP_067637.2:p.Ser121=
XM_011526133.1:c.357+7801T>C	XP_011524435.1:n.357+7801T>C
NM_021624.4:c.363T>C MANE Select	NP_067637.2:p.Ser121=
NM_001143828.2:c.194-95T>C	NP_001137300.1:n.194-95T>C
NM_001160166.2:c.199T>C	NP_001153638.1:p.Leu67=