Canonical Allele Identifier: CA272663675
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1055088
ClinVar RCV Id: RCV002322333 RCV001363700
dbSNP Id: rs1022382647
gnomAD v2: 15-73615268-G-T
gnomAD v3: 15-73322927-G-T
gnomAD v4: 15-73322927-G-T
MyVariant Identifiers: chr15:g.73615268G>T (hg19) chr15:g.73322927G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322927G>T , CM000677.2:g.73322927G>T GRCh38
NC_000015.9:g.73615268G>T , CM000677.1:g.73615268G>T GRCh37
NC_000015.8:g.71402321G>T NCBI36
NG_009063.1:g.51338C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3166C>A MANE Select ENSP00000261917.3:p.Pro1056Thr
ENST00000261917.3:c.3166C>A ENSP00000261917.3:p.Pro1056Thr
NM_005477.2:c.3166C>A NP_005468.1:p.Pro1056Thr
XM_011521148.1:c.1948C>A XP_011519450.1:p.Pro650Thr
XM_011521148.2:c.1948C>A XP_011519450.1:p.Pro650Thr
NM_005477.3:c.3166C>A MANE Select NP_005468.1:p.Pro1056Thr
Search 100 bp 5'
Search 100 bp 3'