Canonical Allele Identifier: CA7649004
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1105591
ClinVar RCV Id: RCV001430008 RCV002456708
dbSNP Id: rs372747050
ExAC: 15:73615896 C / T
gnomAD v2: 15-73615896-C-T
gnomAD v3: 15-73323555-C-T
gnomAD v4: 15-73323555-C-T
COSMIC: COSM1749303
MyVariant Identifiers: chr15:g.73615896C>T (hg19) chr15:g.73323555C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323555C>T , CM000677.2:g.73323555C>T GRCh38
NC_000015.9:g.73615896C>T , CM000677.1:g.73615896C>T GRCh37
NC_000015.8:g.71402949C>T NCBI36
NG_009063.1:g.50710G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2538G>A MANE Select ENSP00000261917.3:p.Pro846=
ENST00000261917.3:c.2538G>A ENSP00000261917.3:p.Pro846=
NM_005477.2:c.2538G>A NP_005468.1:p.Pro846=
XM_011521148.1:c.1320G>A XP_011519450.1:p.Pro440=
XM_011521148.2:c.1320G>A XP_011519450.1:p.Pro440=
NM_005477.3:c.2538G>A MANE Select NP_005468.1:p.Pro846=
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