Canonical Allele Identifier: CA491478706
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1132713
ClinVar RCV Id: RCV001467016
dbSNP Id: rs2151214570
gnomAD v4: 15-73323465-G-A
MyVariant Identifiers: chr15:g.73615806G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323465G>A , CM000677.2:g.73323465G>A GRCh38
NC_000015.9:g.73615806G>A , CM000677.1:g.73615806G>A GRCh37
NC_000015.8:g.71402859G>A NCBI36
NG_009063.1:g.50800C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2628C>T MANE Select ENSP00000261917.3:p.Pro876=
ENST00000261917.3:c.2628C>T ENSP00000261917.3:p.Pro876=
NM_005477.2:c.2628C>T NP_005468.1:p.Pro876=
XM_011521148.1:c.1410C>T XP_011519450.1:p.Pro470=
XM_011521148.2:c.1410C>T XP_011519450.1:p.Pro470=
NM_005477.3:c.2628C>T MANE Select NP_005468.1:p.Pro876=
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