Canonical Allele Identifier: CA491478062
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1550056
ClinVar RCV Id: RCV002175212
dbSNP Id: rs2151213798
gnomAD v3: 15-73322658-G-T
gnomAD v4: 15-73322658-G-T
MyVariant Identifiers: chr15:g.73614999G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322658G>T , CM000677.2:g.73322658G>T GRCh38
NC_000015.9:g.73614999G>T , CM000677.1:g.73614999G>T GRCh37
NC_000015.8:g.71402052G>T NCBI36
NG_009063.1:g.51607C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3435C>A MANE Select ENSP00000261917.3:p.Ile1145=
ENST00000261917.3:c.3435C>A ENSP00000261917.3:p.Ile1145=
NM_005477.2:c.3435C>A NP_005468.1:p.Ile1145=
XM_011521148.1:c.2217C>A XP_011519450.1:p.Ile739=
XM_011521148.2:c.2217C>A XP_011519450.1:p.Ile739=
NM_005477.3:c.3435C>A MANE Select NP_005468.1:p.Ile1145=
Search 100 bp 5'
Search 100 bp 3'