Canonical Allele Identifier: CA988425707
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1909878538

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24469581A>G , CM000680.2:g.24469581A>G GRCh38
NC_000018.9:g.22049545A>G , CM000680.1:g.22049545A>G GRCh37
NC_000018.8:g.20303543A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.357+630A>G MANE Select ENSP00000256906.4:n.357+630A>G
ENST00000256906.4:c.357+630A>G ENSP00000256906.4:n.357+630A>G
ENST00000426880.2:c.194-7266A>G ENSP00000402526.2:n.194-7266A>G
NM_001143828.1:c.194-7266A>G NP_001137300.1:n.194-7266A>G
NM_001160166.1:c.194-7166A>G NP_001153638.1:n.194-7166A>G
NM_021624.3:c.357+630A>G NP_067637.2:n.357+630A>G
XM_011526133.1:c.357+630A>G XP_011524435.1:n.357+630A>G
XM_011526134.1:c.357+630A>G XP_011524436.1:n.357+630A>G
NM_021624.4:c.357+630A>G MANE Select NP_067637.2:n.357+630A>G
NM_001143828.2:c.194-7266A>G NP_001137300.1:n.194-7266A>G
NM_001160166.2:c.194-7166A>G NP_001153638.1:n.194-7166A>G