Canonical Allele Identifier: CA491477920
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322888-G-T
MyVariant Identifiers: chr15:g.73615229G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322888G>T , CM000677.2:g.73322888G>T GRCh38
NC_000015.9:g.73615229G>T , CM000677.1:g.73615229G>T GRCh37
NC_000015.8:g.71402282G>T NCBI36
NG_009063.1:g.51377C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3205C>A MANE Select ENSP00000261917.3:p.Arg1069=
ENST00000261917.3:c.3205C>A ENSP00000261917.3:p.Arg1069=
NM_005477.2:c.3205C>A NP_005468.1:p.Arg1069=
XM_011521148.1:c.1987C>A XP_011519450.1:p.Arg663=
XM_011521148.2:c.1987C>A XP_011519450.1:p.Arg663=
NM_005477.3:c.3205C>A MANE Select NP_005468.1:p.Arg1069=
Search 100 bp 5'
Search 100 bp 3'