Canonical Allele Identifier: CA491478495
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1558826
ClinVar RCV Id: RCV002200229
dbSNP Id: rs375169111
MyVariant Identifiers: chr15:g.73615740G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323399G>T , CM000677.2:g.73323399G>T GRCh38
NC_000015.9:g.73615740G>T , CM000677.1:g.73615740G>T GRCh37
NC_000015.8:g.71402793G>T NCBI36
NG_009063.1:g.50866C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2694C>A MANE Select ENSP00000261917.3:p.Gly898=
ENST00000261917.3:c.2694C>A ENSP00000261917.3:p.Gly898=
NM_005477.2:c.2694C>A NP_005468.1:p.Gly898=
XM_011521148.1:c.1476C>A XP_011519450.1:p.Gly492=
XM_011521148.2:c.1476C>A XP_011519450.1:p.Gly492=
NM_005477.3:c.2694C>A MANE Select NP_005468.1:p.Gly898=
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Search 100 bp 3'