Canonical Allele Identifier: CA393086000
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728957
ClinVar RCV Id: RCV002445435 RCV003099300
gnomAD v4: 15-73322881-G-A
MyVariant Identifiers: chr15:g.73615222G>A (hg19) chr15:g.73322881G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322881G>A , CM000677.2:g.73322881G>A GRCh38
NC_000015.9:g.73615222G>A , CM000677.1:g.73615222G>A GRCh37
NC_000015.8:g.71402275G>A NCBI36
NG_009063.1:g.51384C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3212C>T MANE Select ENSP00000261917.3:p.Thr1071Ile
ENST00000261917.3:c.3212C>T ENSP00000261917.3:p.Thr1071Ile
NM_005477.2:c.3212C>T NP_005468.1:p.Thr1071Ile
XM_011521148.1:c.1994C>T XP_011519450.1:p.Thr665Ile
XM_011521148.2:c.1994C>T XP_011519450.1:p.Thr665Ile
NM_005477.3:c.3212C>T MANE Select NP_005468.1:p.Thr1071Ile
Search 100 bp 5'
Search 100 bp 3'