Canonical Allele Identifier: CA619410594
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1567769877
gnomAD v2: 15-73616383-T-C
gnomAD v3: 15-73324042-T-C
gnomAD v4: 15-73324042-T-C
MyVariant Identifiers: chr15:g.73616383T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324042T>C , CM000677.2:g.73324042T>C GRCh38
NC_000015.9:g.73616383T>C , CM000677.1:g.73616383T>C GRCh37
NC_000015.8:g.71403436T>C NCBI36
NG_009063.1:g.50223A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2143+47A>G MANE Select ENSP00000261917.3:n.2143+47A>G
ENST00000261917.3:c.2143+47A>G ENSP00000261917.3:n.2143+47A>G
NM_005477.2:c.2143+47A>G NP_005468.1:n.2143+47A>G
XM_011521148.1:c.925+47A>G XP_011519450.1:n.925+47A>G
XM_011521148.2:c.925+47A>G XP_011519450.1:n.925+47A>G
NM_005477.3:c.2143+47A>G MANE Select NP_005468.1:n.2143+47A>G
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