Canonical Allele Identifier: CA393093388
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 943336
dbSNP Id: rs1474216387

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329587G>C , CM000677.2:g.73329587G>C GRCh38
NC_000015.9:g.73621928G>C , CM000677.1:g.73621928G>C GRCh37
NC_000015.8:g.71408981G>C NCBI36
NG_009063.1:g.44678C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1576C>G MANE Select ENSP00000261917.3:p.Gln526Glu
ENST00000261917.3:c.1576C>G ENSP00000261917.3:p.Gln526Glu
NM_005477.2:c.1576C>G NP_005468.1:p.Gln526Glu
XM_011521148.1:c.358C>G XP_011519450.1:p.Gln120Glu
XM_011521148.2:c.358C>G XP_011519450.1:p.Gln120Glu
NM_005477.3:c.1576C>G MANE Select NP_005468.1:p.Gln526Glu