Canonical Allele Identifier: CA7648892
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1102318
ClinVar RCV Id: RCV001425566
dbSNP Id: rs774175308
ExAC: 15:73615377 A / G
gnomAD v2: 15-73615377-A-G
gnomAD v4: 15-73323036-A-G
MyVariant Identifiers: chr15:g.73615377A>G (hg19) chr15:g.73323036A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323036A>G , CM000677.2:g.73323036A>G GRCh38
NC_000015.9:g.73615377A>G , CM000677.1:g.73615377A>G GRCh37
NC_000015.8:g.71402430A>G NCBI36
NG_009063.1:g.51229T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3057T>C MANE Select ENSP00000261917.3:p.Phe1019=
ENST00000261917.3:c.3057T>C ENSP00000261917.3:p.Phe1019=
NM_005477.2:c.3057T>C NP_005468.1:p.Phe1019=
XM_011521148.1:c.1839T>C XP_011519450.1:p.Phe613=
XM_011521148.2:c.1839T>C XP_011519450.1:p.Phe613=
NM_005477.3:c.3057T>C MANE Select NP_005468.1:p.Phe1019=
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