Canonical Allele Identifier: CA619080160
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1318182514
gnomAD v2: 15-73622456-C-T
gnomAD v3: 15-73330115-C-T
gnomAD v4: 15-73330115-C-T
MyVariant Identifiers: chr15:g.73622456C>T (hg19) chr15:g.73330115C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330115C>T , CM000677.2:g.73330115C>T GRCh38
NC_000015.9:g.73622456C>T , CM000677.1:g.73622456C>T GRCh37
NC_000015.8:g.71409509C>T NCBI36
NG_009063.1:g.44150G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-324G>A MANE Select ENSP00000261917.3:n.1372-324G>A
ENST00000261917.3:c.1372-324G>A ENSP00000261917.3:n.1372-324G>A
NM_005477.2:c.1372-324G>A NP_005468.1:n.1372-324G>A
XM_011521148.1:c.154-324G>A XP_011519450.1:n.154-324G>A
XM_011521148.2:c.154-324G>A XP_011519450.1:n.154-324G>A
NM_005477.3:c.1372-324G>A MANE Select NP_005468.1:n.1372-324G>A
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