Canonical Allele Identifier: CA272700156
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1055534495
gnomAD v4: 15-73367676-G-C
MyVariant Identifiers: chr15:g.73660017G>C (hg19) chr15:g.73367676G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367676G>C , CM000677.2:g.73367676G>C GRCh38
NC_000015.9:g.73660017G>C , CM000677.1:g.73660017G>C GRCh37
NC_000015.8:g.71447070G>C NCBI36
NG_009063.1:g.6589C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.595C>G MANE Select ENSP00000261917.3:p.Gln199Glu
ENST00000261917.3:c.595C>G ENSP00000261917.3:p.Gln199Glu
NM_005477.2:c.595C>G NP_005468.1:p.Gln199Glu
NM_005477.3:c.595C>G MANE Select NP_005468.1:p.Gln199Glu
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Search 100 bp 3'