Canonical Allele Identifier: CA503523685

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22057100T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477136T>C , CM000680.2:g.24477136T>C	GRCh38
NC_000018.9:g.22057100T>C , CM000680.1:g.22057100T>C	GRCh37
NC_000018.8:g.20311098T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.747T>C MANE Select	ENSP00000256906.4:p.His249=
ENST00000256906.4:c.747T>C	ENSP00000256906.4:p.His249=
ENST00000426880.2:c.483T>C	ENSP00000402526.2:p.His161=
NM_001143828.1:c.483T>C	NP_001137300.1:p.His161=
NM_001160166.1:c.*379T>C	NP_001153638.1:n.*379T>C
NM_021624.3:c.747T>C	NP_067637.2:p.His249=
XM_011526133.1:c.357+8185T>C	XP_011524435.1:n.357+8185T>C
NM_021624.4:c.747T>C MANE Select	NP_067637.2:p.His249=
NM_001143828.2:c.483T>C	NP_001137300.1:p.His161=
NM_001160166.2:c.*379T>C	NP_001153638.1:n.*379T>C