Canonical Allele Identifier: CA393098704
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786228
ClinVar RCV Id: RCV002417605
dbSNP Id: rs1360146681
gnomAD v2: 15-73660401-C-T
gnomAD v4: 15-73368060-C-T
MyVariant Identifiers: chr15:g.73660401C>T (hg19) chr15:g.73368060C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368060C>T , CM000677.2:g.73368060C>T GRCh38
NC_000015.9:g.73660401C>T , CM000677.1:g.73660401C>T GRCh37
NC_000015.8:g.71447454C>T NCBI36
NG_009063.1:g.6205G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.211G>A MANE Select ENSP00000261917.3:p.Ala71Thr
ENST00000261917.3:c.211G>A ENSP00000261917.3:p.Ala71Thr
NM_005477.2:c.211G>A NP_005468.1:p.Ala71Thr
NM_005477.3:c.211G>A MANE Select NP_005468.1:p.Ala71Thr
Search 100 bp 5'
Search 100 bp 3'