Canonical Allele Identifier: CA393085887
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517361
ClinVar RCV Id: RCV002027297
dbSNP Id: rs1050326641
gnomAD v4: 15-73322831-C-G
MyVariant Identifiers: chr15:g.73615172C>G (hg19) chr15:g.73322831C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322831C>G , CM000677.2:g.73322831C>G GRCh38
NC_000015.9:g.73615172C>G , CM000677.1:g.73615172C>G GRCh37
NC_000015.8:g.71402225C>G NCBI36
NG_009063.1:g.51434G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3262G>C MANE Select ENSP00000261917.3:p.Ala1088Pro
ENST00000261917.3:c.3262G>C ENSP00000261917.3:p.Ala1088Pro
NM_005477.2:c.3262G>C NP_005468.1:p.Ala1088Pro
XM_011521148.1:c.2044G>C XP_011519450.1:p.Ala682Pro
XM_011521148.2:c.2044G>C XP_011519450.1:p.Ala682Pro
NM_005477.3:c.3262G>C MANE Select NP_005468.1:p.Ala1088Pro
Search 100 bp 5'
Search 100 bp 3'