Canonical Allele Identifier: CA393097395
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73659974A>T (hg19) chr15:g.73367633A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367633A>T , CM000677.2:g.73367633A>T GRCh38
NC_000015.9:g.73659974A>T , CM000677.1:g.73659974A>T GRCh37
NC_000015.8:g.71447027A>T NCBI36
NG_009063.1:g.6632T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.638T>A MANE Select ENSP00000261917.3:p.Phe213Tyr
ENST00000261917.3:c.638T>A ENSP00000261917.3:p.Phe213Tyr
NM_005477.2:c.638T>A NP_005468.1:p.Phe213Tyr
NM_005477.3:c.638T>A MANE Select NP_005468.1:p.Phe213Tyr
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