Canonical Allele Identifier: CA393086201
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773159
ClinVar RCV Id: RCV003505752
MyVariant Identifiers: chr15:g.73615326T>A (hg19) chr15:g.73322985T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322985T>A , CM000677.2:g.73322985T>A GRCh38
NC_000015.9:g.73615326T>A , CM000677.1:g.73615326T>A GRCh37
NC_000015.8:g.71402379T>A NCBI36
NG_009063.1:g.51280A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3108A>T MANE Select ENSP00000261917.3:p.Arg1036Ser
ENST00000261917.3:c.3108A>T ENSP00000261917.3:p.Arg1036Ser
NM_005477.2:c.3108A>T NP_005468.1:p.Arg1036Ser
XM_011521148.1:c.1890A>T XP_011519450.1:p.Arg630Ser
XM_011521148.2:c.1890A>T XP_011519450.1:p.Arg630Ser
NM_005477.3:c.3108A>T MANE Select NP_005468.1:p.Arg1036Ser
Search 100 bp 5'
Search 100 bp 3'