Canonical Allele Identifier: CA393095232
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1307595
ClinVar RCV Id: RCV001763131
dbSNP Id: rs2151221234
MyVariant Identifiers: chr15:g.73636008G>C (hg19) chr15:g.73343667G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343667G>C , CM000677.2:g.73343667G>C GRCh38
NC_000015.9:g.73636008G>C , CM000677.1:g.73636008G>C GRCh37
NC_000015.8:g.71423061G>C NCBI36
NG_009063.1:g.30598C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.927C>G MANE Select ENSP00000261917.3:p.Asp309Glu
ENST00000261917.3:c.927C>G ENSP00000261917.3:p.Asp309Glu
NM_005477.2:c.927C>G NP_005468.1:p.Asp309Glu
NM_005477.3:c.927C>G MANE Select NP_005468.1:p.Asp309Glu
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