Canonical Allele Identifier: CA491479498
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 518880
ClinVar RCV Id: RCV000618186
dbSNP Id: rs1555478937
COSMIC: COSM4829565
MyVariant Identifiers: chr15:g.73659973G>A (hg19) chr15:g.73367632G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367632G>A , CM000677.2:g.73367632G>A GRCh38
NC_000015.9:g.73659973G>A , CM000677.1:g.73659973G>A GRCh37
NC_000015.8:g.71447026G>A NCBI36
NG_009063.1:g.6633C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.639C>T MANE Select ENSP00000261917.3:p.Phe213=
ENST00000261917.3:c.639C>T ENSP00000261917.3:p.Phe213=
NM_005477.2:c.639C>T NP_005468.1:p.Phe213=
NM_005477.3:c.639C>T MANE Select NP_005468.1:p.Phe213=
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