Canonical Allele Identifier: CA777784965
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1273924853
MyVariant Identifiers: chr18:g.22040674T>A (hg19) chr18:g.24460710T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460710T>A , CM000680.2:g.24460710T>A GRCh38
NC_000018.9:g.22040674T>A , CM000680.1:g.22040674T>A GRCh37
NC_000018.8:g.20294672T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.-19T>A MANE Select ENSP00000256906.4:n.-19T>A
ENST00000256906.4:c.-19T>A ENSP00000256906.4:n.-19T>A
NM_001143828.1:c.-19T>A NP_001137300.1:n.-19T>A
NM_001160166.1:c.-19T>A NP_001153638.1:n.-19T>A
NM_021624.3:c.-19T>A NP_067637.2:n.-19T>A
XM_011526133.1:c.-19T>A XP_011524435.1:n.-19T>A
XM_011526134.1:c.-19T>A XP_011524436.1:n.-19T>A
NM_021624.4:c.-19T>A MANE Select NP_067637.2:n.-19T>A
NM_001143828.2:c.-19T>A NP_001137300.1:n.-19T>A
NM_001160166.2:c.-19T>A NP_001153638.1:n.-19T>A
Search 100 bp 5'
Search 100 bp 3'