Canonical Allele Identifier: CA491479502
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1084397
ClinVar RCV Id: RCV001401381
dbSNP Id: rs545040345
MyVariant Identifiers: chr15:g.73659979G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367638G>C , CM000677.2:g.73367638G>C GRCh38
NC_000015.9:g.73659979G>C , CM000677.1:g.73659979G>C GRCh37
NC_000015.8:g.71447032G>C NCBI36
NG_009063.1:g.6627C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.633C>G MANE Select ENSP00000261917.3:p.Ala211=
ENST00000261917.3:c.633C>G ENSP00000261917.3:p.Ala211=
NM_005477.2:c.633C>G NP_005468.1:p.Ala211=
NM_005477.3:c.633C>G MANE Select NP_005468.1:p.Ala211=
Search 100 bp 5'
Search 100 bp 3'