Canonical Allele Identifier: CA393086017
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728836
ClinVar RCV Id: RCV002443360 RCV003099290
gnomAD v4: 15-73322891-G-T
MyVariant Identifiers: chr15:g.73615232G>T (hg19) chr15:g.73322891G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322891G>T , CM000677.2:g.73322891G>T GRCh38
NC_000015.9:g.73615232G>T , CM000677.1:g.73615232G>T GRCh37
NC_000015.8:g.71402285G>T NCBI36
NG_009063.1:g.51374C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3202C>A MANE Select ENSP00000261917.3:p.Arg1068Ser
ENST00000261917.3:c.3202C>A ENSP00000261917.3:p.Arg1068Ser
NM_005477.2:c.3202C>A NP_005468.1:p.Arg1068Ser
XM_011521148.1:c.1984C>A XP_011519450.1:p.Arg662Ser
XM_011521148.2:c.1984C>A XP_011519450.1:p.Arg662Ser
NM_005477.3:c.3202C>A MANE Select NP_005468.1:p.Arg1068Ser
Search 100 bp 5'
Search 100 bp 3'