Canonical Allele Identifier: CA402082468
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22056727A>C (hg19) chr18:g.24476763A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476763A>C , CM000680.2:g.24476763A>C GRCh38
NC_000018.9:g.22056727A>C , CM000680.1:g.22056727A>C GRCh37
NC_000018.8:g.20310725A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.374A>C MANE Select ENSP00000256906.4:p.Gln125Pro
ENST00000256906.4:c.374A>C ENSP00000256906.4:p.Gln125Pro
ENST00000426880.2:c.194-84A>C ENSP00000402526.2:n.194-84A>C
NM_001143828.1:c.194-84A>C NP_001137300.1:n.194-84A>C
NM_001160166.1:c.*6A>C NP_001153638.1:n.*6A>C
NM_021624.3:c.374A>C NP_067637.2:p.Gln125Pro
XM_011526133.1:c.357+7812A>C XP_011524435.1:n.357+7812A>C
NM_021624.4:c.374A>C MANE Select NP_067637.2:p.Gln125Pro
NM_001143828.2:c.194-84A>C NP_001137300.1:n.194-84A>C
NM_001160166.2:c.*6A>C NP_001153638.1:n.*6A>C
Search 100 bp 5'
Search 100 bp 3'