Canonical Allele Identifier: CA393095037
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73635919T>A (hg19) chr15:g.73343578T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343578T>A , CM000677.2:g.73343578T>A GRCh38
NC_000015.9:g.73635919T>A , CM000677.1:g.73635919T>A GRCh37
NC_000015.8:g.71422972T>A NCBI36
NG_009063.1:g.30687A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1016A>T MANE Select ENSP00000261917.3:p.Lys339Ile
ENST00000261917.3:c.1016A>T ENSP00000261917.3:p.Lys339Ile
NM_005477.2:c.1016A>T NP_005468.1:p.Lys339Ile
NM_005477.3:c.1016A>T MANE Select NP_005468.1:p.Lys339Ile
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