Canonical Allele Identifier: CA393095256
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73636018A>G (hg19) chr15:g.73343677A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343677A>G , CM000677.2:g.73343677A>G GRCh38
NC_000015.9:g.73636018A>G , CM000677.1:g.73636018A>G GRCh37
NC_000015.8:g.71423071A>G NCBI36
NG_009063.1:g.30588T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.917T>C MANE Select ENSP00000261917.3:p.Phe306Ser
ENST00000261917.3:c.917T>C ENSP00000261917.3:p.Phe306Ser
NM_005477.2:c.917T>C NP_005468.1:p.Phe306Ser
NM_005477.3:c.917T>C MANE Select NP_005468.1:p.Phe306Ser
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