Canonical Allele Identifier: CA491479826
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2770364
ClinVar RCV Id: RCV003505669
MyVariant Identifiers: chr15:g.73636002G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343661G>A , CM000677.2:g.73343661G>A GRCh38
NC_000015.9:g.73636002G>A , CM000677.1:g.73636002G>A GRCh37
NC_000015.8:g.71423055G>A NCBI36
NG_009063.1:g.30604C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.933C>T MANE Select ENSP00000261917.3:p.Val311=
ENST00000261917.3:c.933C>T ENSP00000261917.3:p.Val311=
NM_005477.2:c.933C>T NP_005468.1:p.Val311=
NM_005477.3:c.933C>T MANE Select NP_005468.1:p.Val311=
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