Canonical Allele Identifier: CA393085330
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042867733
gnomAD v3: 15-73322660-T-A
gnomAD v4: 15-73322660-T-A
MyVariant Identifiers: chr15:g.73615001T>A (hg19) chr15:g.73322660T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322660T>A , CM000677.2:g.73322660T>A GRCh38
NC_000015.9:g.73615001T>A , CM000677.1:g.73615001T>A GRCh37
NC_000015.8:g.71402054T>A NCBI36
NG_009063.1:g.51605A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3433A>T MANE Select ENSP00000261917.3:p.Ile1145Phe
ENST00000261917.3:c.3433A>T ENSP00000261917.3:p.Ile1145Phe
NM_005477.2:c.3433A>T NP_005468.1:p.Ile1145Phe
XM_011521148.1:c.2215A>T XP_011519450.1:p.Ile739Phe
XM_011521148.2:c.2215A>T XP_011519450.1:p.Ile739Phe
NM_005477.3:c.3433A>T MANE Select NP_005468.1:p.Ile1145Phe
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