Canonical Allele Identifier: CA402083189

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22057002A>T (hg19) ; chr18:g.24477038A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477038A>T , CM000680.2:g.24477038A>T	GRCh38
NC_000018.9:g.22057002A>T , CM000680.1:g.22057002A>T	GRCh37
NC_000018.8:g.20311000A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.649A>T MANE Select	ENSP00000256906.4:p.Thr217Ser
ENST00000256906.4:c.649A>T	ENSP00000256906.4:p.Thr217Ser
ENST00000426880.2:c.385A>T	ENSP00000402526.2:p.Thr129Ser
NM_001143828.1:c.385A>T	NP_001137300.1:p.Thr129Ser
NM_001160166.1:c.*281A>T	NP_001153638.1:n.*281A>T
NM_021624.3:c.649A>T	NP_067637.2:p.Thr217Ser
XM_011526133.1:c.357+8087A>T	XP_011524435.1:n.357+8087A>T
NM_021624.4:c.649A>T MANE Select	NP_067637.2:p.Thr217Ser
NM_001143828.2:c.385A>T	NP_001137300.1:p.Thr129Ser
NM_001160166.2:c.*281A>T	NP_001153638.1:n.*281A>T