Canonical Allele Identifier: CA393094264
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003826
ClinVar RCV Id: RCV001300435
dbSNP Id: rs1394017911
gnomAD v2: 15-73624486-T-C
gnomAD v4: 15-73332145-T-C
COSMIC: COSM5683096
MyVariant Identifiers: chr15:g.73624486T>C (hg19) chr15:g.73332145T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332145T>C , CM000677.2:g.73332145T>C GRCh38
NC_000015.9:g.73624486T>C , CM000677.1:g.73624486T>C GRCh37
NC_000015.8:g.71411539T>C NCBI36
NG_009063.1:g.42120A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1357A>G MANE Select ENSP00000261917.3:p.Ile453Val
ENST00000261917.3:c.1357A>G ENSP00000261917.3:p.Ile453Val
NM_005477.2:c.1357A>G NP_005468.1:p.Ile453Val
XM_011521148.1:c.139A>G XP_011519450.1:p.Ile47Val
XM_011521148.2:c.139A>G XP_011519450.1:p.Ile47Val
NM_005477.3:c.1357A>G MANE Select NP_005468.1:p.Ile453Val
Search 100 bp 5'
Search 100 bp 3'