Canonical Allele Identifier: CA2187167938
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1595823113
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330090T>G , CM000677.2:g.73330090T>G GRCh38
NC_000015.9:g.73622431T>G , CM000677.1:g.73622431T>G GRCh37
NC_000015.8:g.71409484T>G NCBI36
NG_009063.1:g.44175A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-299A>C MANE Select ENSP00000261917.3:n.1372-299A>C
ENST00000261917.3:c.1372-299A>C ENSP00000261917.3:n.1372-299A>C
NM_005477.2:c.1372-299A>C NP_005468.1:n.1372-299A>C
XM_011521148.1:c.154-299A>C XP_011519450.1:n.154-299A>C
XM_011521148.2:c.154-299A>C XP_011519450.1:n.154-299A>C
NM_005477.3:c.1372-299A>C MANE Select NP_005468.1:n.1372-299A>C
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