Canonical Allele Identifier: CA272663688
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 643830
ClinVar RCV Id: RCV000797624 RCV002325525
dbSNP Id: rs980750316
gnomAD v2: 15-73615300-G-A
gnomAD v3: 15-73322959-G-A
gnomAD v4: 15-73322959-G-A
MyVariant Identifiers: chr15:g.73615300G>A (hg19) chr15:g.73322959G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322959G>A , CM000677.2:g.73322959G>A GRCh38
NC_000015.9:g.73615300G>A , CM000677.1:g.73615300G>A GRCh37
NC_000015.8:g.71402353G>A NCBI36
NG_009063.1:g.51306C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3134C>T MANE Select ENSP00000261917.3:p.Ala1045Val
ENST00000261917.3:c.3134C>T ENSP00000261917.3:p.Ala1045Val
NM_005477.2:c.3134C>T NP_005468.1:p.Ala1045Val
XM_011521148.1:c.1916C>T XP_011519450.1:p.Ala639Val
XM_011521148.2:c.1916C>T XP_011519450.1:p.Ala639Val
NM_005477.3:c.3134C>T MANE Select NP_005468.1:p.Ala1045Val
Search 100 bp 5'
Search 100 bp 3'