Canonical Allele Identifier: CA491478826
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1797219
ClinVar RCV Id: RCV002437844
dbSNP Id: rs2151214312
gnomAD v4: 15-73323207-T-G
MyVariant Identifiers: chr15:g.73615548T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323207T>G , CM000677.2:g.73323207T>G GRCh38
NC_000015.9:g.73615548T>G , CM000677.1:g.73615548T>G GRCh37
NC_000015.8:g.71402601T>G NCBI36
NG_009063.1:g.51058A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2886A>C MANE Select ENSP00000261917.3:p.Pro962=
ENST00000261917.3:c.2886A>C ENSP00000261917.3:p.Pro962=
NM_005477.2:c.2886A>C NP_005468.1:p.Pro962=
XM_011521148.1:c.1668A>C XP_011519450.1:p.Pro556=
XM_011521148.2:c.1668A>C XP_011519450.1:p.Pro556=
NM_005477.3:c.2886A>C MANE Select NP_005468.1:p.Pro962=
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