Canonical Allele Identifier: CA491478545
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1609076
ClinVar RCV Id: RCV002150030
dbSNP Id: rs1333164922
MyVariant Identifiers: chr15:g.73616058G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323717G>C , CM000677.2:g.73323717G>C GRCh38
NC_000015.9:g.73616058G>C , CM000677.1:g.73616058G>C GRCh37
NC_000015.8:g.71403111G>C NCBI36
NG_009063.1:g.50548C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2376C>G MANE Select ENSP00000261917.3:p.Ala792=
ENST00000261917.3:c.2376C>G ENSP00000261917.3:p.Ala792=
NM_005477.2:c.2376C>G NP_005468.1:p.Ala792=
XM_011521148.1:c.1158C>G XP_011519450.1:p.Ala386=
XM_011521148.2:c.1158C>G XP_011519450.1:p.Ala386=
NM_005477.3:c.2376C>G MANE Select NP_005468.1:p.Ala792=
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