Canonical Allele Identifier: CA491478718
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1534026
ClinVar RCV Id: RCV002071484 RCV003303691
dbSNP Id: rs1160062560
gnomAD v2: 15-73615811-G-A
MyVariant Identifiers: chr15:g.73615811G>A (hg19) chr15:g.73323470G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323470G>A , CM000677.2:g.73323470G>A GRCh38
NC_000015.9:g.73615811G>A , CM000677.1:g.73615811G>A GRCh37
NC_000015.8:g.71402864G>A NCBI36
NG_009063.1:g.50795C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2623C>T MANE Select ENSP00000261917.3:p.Leu875=
ENST00000261917.3:c.2623C>T ENSP00000261917.3:p.Leu875=
NM_005477.2:c.2623C>T NP_005468.1:p.Leu875=
XM_011521148.1:c.1405C>T XP_011519450.1:p.Leu469=
XM_011521148.2:c.1405C>T XP_011519450.1:p.Leu469=
NM_005477.3:c.2623C>T MANE Select NP_005468.1:p.Leu875=
Search 100 bp 5'
Search 100 bp 3'