Canonical Allele Identifier: CA402083578
Gene: HRH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477218G>T , CM000680.2:g.24477218G>T GRCh38
NC_000018.9:g.22057182G>T , CM000680.1:g.22057182G>T GRCh37
NC_000018.8:g.20311180G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.829G>T MANE Select ENSP00000256906.4:p.Gly277Cys
ENST00000256906.4:c.829G>T ENSP00000256906.4:p.Gly277Cys
ENST00000426880.2:c.565G>T ENSP00000402526.2:p.Gly189Cys
NM_001143828.1:c.565G>T NP_001137300.1:p.Gly189Cys
NM_001160166.1:c.*461G>T NP_001153638.1:n.*461G>T
NM_021624.3:c.829G>T NP_067637.2:p.Gly277Cys
XM_011526133.1:c.357+8267G>T XP_011524435.1:n.357+8267G>T
NM_021624.4:c.829G>T MANE Select NP_067637.2:p.Gly277Cys
NM_001143828.2:c.565G>T NP_001137300.1:p.Gly189Cys
NM_001160166.2:c.*461G>T NP_001153638.1:n.*461G>T