Canonical Allele Identifier: CA7649447
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1548779
ClinVar RCV Id: RCV002187113 RCV002361437
dbSNP Id: rs545040345
ExAC: 15:73659979 G / T
gnomAD v2: 15-73659979-G-T
gnomAD v3: 15-73367638-G-T
gnomAD v4: 15-73367638-G-T
MyVariant Identifiers: chr15:g.73659979G>T (hg19) chr15:g.73367638G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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