Canonical Allele Identifier: CA7648895
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1799183
ClinVar RCV Id: RCV002444030
dbSNP Id: rs750605160
ExAC: 15:73615390 G / C
gnomAD v4: 15-73323049-G-C
MyVariant Identifiers: chr15:g.73615390G>C (hg19) chr15:g.73323049G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323049G>C , CM000677.2:g.73323049G>C GRCh38
NC_000015.9:g.73615390G>C , CM000677.1:g.73615390G>C GRCh37
NC_000015.8:g.71402443G>C NCBI36
NG_009063.1:g.51216C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3044C>G MANE Select ENSP00000261917.3:p.Ser1015Cys
ENST00000261917.3:c.3044C>G ENSP00000261917.3:p.Ser1015Cys
NM_005477.2:c.3044C>G NP_005468.1:p.Ser1015Cys
XM_011521148.1:c.1826C>G XP_011519450.1:p.Ser609Cys
XM_011521148.2:c.1826C>G XP_011519450.1:p.Ser609Cys
NM_005477.3:c.3044C>G MANE Select NP_005468.1:p.Ser1015Cys
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