Canonical Allele Identifier: CA491478124
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 886650
ClinVar RCV Id: RCV001118931 RCV001493020 RCV002319663
dbSNP Id: rs1226393084
gnomAD v2: 15-73615353-G-A
gnomAD v3: 15-73323012-G-A
gnomAD v4: 15-73323012-G-A
MyVariant Identifiers: chr15:g.73615353G>A (hg19) chr15:g.73323012G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323012G>A , CM000677.2:g.73323012G>A GRCh38
NC_000015.9:g.73615353G>A , CM000677.1:g.73615353G>A GRCh37
NC_000015.8:g.71402406G>A NCBI36
NG_009063.1:g.51253C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3081C>T MANE Select ENSP00000261917.3:p.Pro1027=
ENST00000261917.3:c.3081C>T ENSP00000261917.3:p.Pro1027=
NM_005477.2:c.3081C>T NP_005468.1:p.Pro1027=
XM_011521148.1:c.1863C>T XP_011519450.1:p.Pro621=
XM_011521148.2:c.1863C>T XP_011519450.1:p.Pro621=
NM_005477.3:c.3081C>T MANE Select NP_005468.1:p.Pro1027=
Search 100 bp 5'
Search 100 bp 3'