Canonical Allele Identifier: CA491479401
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626618
ClinVar RCV Id: RCV003384158 RCV003614234
gnomAD v4: 15-73367992-G-A
MyVariant Identifiers: chr15:g.73660333G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367992G>A , CM000677.2:g.73367992G>A GRCh38
NC_000015.9:g.73660333G>A , CM000677.1:g.73660333G>A GRCh37
NC_000015.8:g.71447386G>A NCBI36
NG_009063.1:g.6273C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.279C>T MANE Select ENSP00000261917.3:p.Cys93=
ENST00000261917.3:c.279C>T ENSP00000261917.3:p.Cys93=
NM_005477.2:c.279C>T NP_005468.1:p.Cys93=
NM_005477.3:c.279C>T MANE Select NP_005468.1:p.Cys93=
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