Canonical Allele Identifier: CA491151729
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1383219143
gnomAD v2: 15-73622055-C-T
gnomAD v4: 15-73329714-C-T
MyVariant Identifiers: chr15:g.73622055C>T (hg19) chr15:g.73329714C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329714C>T , CM000677.2:g.73329714C>T GRCh38
NC_000015.9:g.73622055C>T , CM000677.1:g.73622055C>T GRCh37
NC_000015.8:g.71409108C>T NCBI36
NG_009063.1:g.44551G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1449G>A MANE Select ENSP00000261917.3:p.Arg483=
ENST00000261917.3:c.1449G>A ENSP00000261917.3:p.Arg483=
NM_005477.2:c.1449G>A NP_005468.1:p.Arg483=
XM_011521148.1:c.231G>A XP_011519450.1:p.Arg77=
XM_011521148.2:c.231G>A XP_011519450.1:p.Arg77=
NM_005477.3:c.1449G>A MANE Select NP_005468.1:p.Arg483=
Search 100 bp 5'
Search 100 bp 3'