Canonical Allele Identifier: CA393093408
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2885201
ClinVar RCV Id: RCV003615134
dbSNP Id: rs756855616
gnomAD v4: 15-73329593-G-A
MyVariant Identifiers: chr15:g.73621934G>A (hg19) chr15:g.73329593G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329593G>A , CM000677.2:g.73329593G>A GRCh38
NC_000015.9:g.73621934G>A , CM000677.1:g.73621934G>A GRCh37
NC_000015.8:g.71408987G>A NCBI36
NG_009063.1:g.44672C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1570C>T MANE Select ENSP00000261917.3:p.Arg524Trp
ENST00000261917.3:c.1570C>T ENSP00000261917.3:p.Arg524Trp
NM_005477.2:c.1570C>T NP_005468.1:p.Arg524Trp
XM_011521148.1:c.352C>T XP_011519450.1:p.Arg118Trp
XM_011521148.2:c.352C>T XP_011519450.1:p.Arg118Trp
NM_005477.3:c.1570C>T MANE Select NP_005468.1:p.Arg524Trp
Search 100 bp 5'
Search 100 bp 3'