Canonical Allele Identifier: CA491151571
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 699040
ClinVar RCV Id: RCV001430424 RCV002390776
dbSNP Id: rs1260804406
gnomAD v2: 15-73622013-G-A
gnomAD v3: 15-73329672-G-A
gnomAD v4: 15-73329672-G-A
MyVariant Identifiers: chr15:g.73622013G>A (hg19) chr15:g.73329672G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329672G>A , CM000677.2:g.73329672G>A GRCh38
NC_000015.9:g.73622013G>A , CM000677.1:g.73622013G>A GRCh37
NC_000015.8:g.71409066G>A NCBI36
NG_009063.1:g.44593C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1491C>T MANE Select ENSP00000261917.3:p.Leu497=
ENST00000261917.3:c.1491C>T ENSP00000261917.3:p.Leu497=
NM_005477.2:c.1491C>T NP_005468.1:p.Leu497=
XM_011521148.1:c.273C>T XP_011519450.1:p.Leu91=
XM_011521148.2:c.273C>T XP_011519450.1:p.Leu91=
NM_005477.3:c.1491C>T MANE Select NP_005468.1:p.Leu497=
Search 100 bp 5'
Search 100 bp 3'