Canonical Allele Identifier: CA7648979
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 948442
ClinVar RCV Id: RCV001219696
dbSNP Id: rs757066783
ExAC: 15:73615781 C / T
gnomAD v2: 15-73615781-C-T
gnomAD v3: 15-73323440-C-T
gnomAD v4: 15-73323440-C-T
COSMIC: COSM4623165
MyVariant Identifiers: chr15:g.73615781C>T (hg19) chr15:g.73323440C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323440C>T , CM000677.2:g.73323440C>T GRCh38
NC_000015.9:g.73615781C>T , CM000677.1:g.73615781C>T GRCh37
NC_000015.8:g.71402834C>T NCBI36
NG_009063.1:g.50825G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2653G>A MANE Select ENSP00000261917.3:p.Gly885Arg
ENST00000261917.3:c.2653G>A ENSP00000261917.3:p.Gly885Arg
NM_005477.2:c.2653G>A NP_005468.1:p.Gly885Arg
XM_011521148.1:c.1435G>A XP_011519450.1:p.Gly479Arg
XM_011521148.2:c.1435G>A XP_011519450.1:p.Gly479Arg
NM_005477.3:c.2653G>A MANE Select NP_005468.1:p.Gly885Arg
Search 100 bp 5'
Search 100 bp 3'