Canonical Allele Identifier: CA272663655
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2085100
ClinVar RCV Id: RCV002996103 RCV004068459
dbSNP Id: rs1010963303
gnomAD v2: 15-73615252-G-A
gnomAD v4: 15-73322911-G-A
MyVariant Identifiers: chr15:g.73615252G>A (hg19) chr15:g.73322911G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322911G>A , CM000677.2:g.73322911G>A GRCh38
NC_000015.9:g.73615252G>A , CM000677.1:g.73615252G>A GRCh37
NC_000015.8:g.71402305G>A NCBI36
NG_009063.1:g.51354C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3182C>T MANE Select ENSP00000261917.3:p.Pro1061Leu
ENST00000261917.3:c.3182C>T ENSP00000261917.3:p.Pro1061Leu
NM_005477.2:c.3182C>T NP_005468.1:p.Pro1061Leu
XM_011521148.1:c.1964C>T XP_011519450.1:p.Pro655Leu
XM_011521148.2:c.1964C>T XP_011519450.1:p.Pro655Leu
NM_005477.3:c.3182C>T MANE Select NP_005468.1:p.Pro1061Leu
Search 100 bp 5'
Search 100 bp 3'