Canonical Allele Identifier: CA393095350
Gene: HCN4 HGNC NCBI

Linked Data

COSMIC: COSM5024377
MyVariant Identifiers: chr15:g.73636060G>A (hg19) chr15:g.73343719G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343719G>A , CM000677.2:g.73343719G>A GRCh38
NC_000015.9:g.73636060G>A , CM000677.1:g.73636060G>A GRCh37
NC_000015.8:g.71423113G>A NCBI36
NG_009063.1:g.30546C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.875C>T MANE Select ENSP00000261917.3:p.Thr292Ile
ENST00000261917.3:c.875C>T ENSP00000261917.3:p.Thr292Ile
NM_005477.2:c.875C>T NP_005468.1:p.Thr292Ile
NM_005477.3:c.875C>T MANE Select NP_005468.1:p.Thr292Ile
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Search 100 bp 3'