Canonical Allele Identifier: CA491478792
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3001771
ClinVar RCV Id: RCV003862834
MyVariant Identifiers: chr15:g.73615538T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323197T>G , CM000677.2:g.73323197T>G GRCh38
NC_000015.9:g.73615538T>G , CM000677.1:g.73615538T>G GRCh37
NC_000015.8:g.71402591T>G NCBI36
NG_009063.1:g.51068A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2896A>C MANE Select ENSP00000261917.3:p.Arg966=
ENST00000261917.3:c.2896A>C ENSP00000261917.3:p.Arg966=
NM_005477.2:c.2896A>C NP_005468.1:p.Arg966=
XM_011521148.1:c.1678A>C XP_011519450.1:p.Arg560=
XM_011521148.2:c.1678A>C XP_011519450.1:p.Arg560=
NM_005477.3:c.2896A>C MANE Select NP_005468.1:p.Arg966=
Search 100 bp 5'
Search 100 bp 3'