Canonical Allele Identifier: CA393085353
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615008A>T (hg19) chr15:g.73322667A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322667A>T , CM000677.2:g.73322667A>T GRCh38
NC_000015.9:g.73615008A>T , CM000677.1:g.73615008A>T GRCh37
NC_000015.8:g.71402061A>T NCBI36
NG_009063.1:g.51598T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3426T>A MANE Select ENSP00000261917.3:p.Tyr1142Ter
ENST00000261917.3:c.3426T>A ENSP00000261917.3:p.Tyr1142Ter
NM_005477.2:c.3426T>A NP_005468.1:p.Tyr1142Ter
XM_011521148.1:c.2208T>A XP_011519450.1:p.Tyr736Ter
XM_011521148.2:c.2208T>A XP_011519450.1:p.Tyr736Ter
NM_005477.3:c.3426T>A MANE Select NP_005468.1:p.Tyr1142Ter
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