Canonical Allele Identifier: CA393097615
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660045T>A (hg19) chr15:g.73367704T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367704T>A , CM000677.2:g.73367704T>A GRCh38
NC_000015.9:g.73660045T>A , CM000677.1:g.73660045T>A GRCh37
NC_000015.8:g.71447098T>A NCBI36
NG_009063.1:g.6561A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.567A>T MANE Select ENSP00000261917.3:p.Lys189Asn
ENST00000261917.3:c.567A>T ENSP00000261917.3:p.Lys189Asn
NM_005477.2:c.567A>T NP_005468.1:p.Lys189Asn
NM_005477.3:c.567A>T MANE Select NP_005468.1:p.Lys189Asn
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Search 100 bp 3'