Canonical Allele Identifier: CA393085390
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719643
ClinVar RCV Id: RCV002303885
MyVariant Identifiers: chr15:g.73615028C>A (hg19) chr15:g.73322687C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322687C>A , CM000677.2:g.73322687C>A GRCh38
NC_000015.9:g.73615028C>A , CM000677.1:g.73615028C>A GRCh37
NC_000015.8:g.71402081C>A NCBI36
NG_009063.1:g.51578G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3406G>T MANE Select ENSP00000261917.3:p.Gly1136Cys
ENST00000261917.3:c.3406G>T ENSP00000261917.3:p.Gly1136Cys
NM_005477.2:c.3406G>T NP_005468.1:p.Gly1136Cys
XM_011521148.1:c.2188G>T XP_011519450.1:p.Gly730Cys
XM_011521148.2:c.2188G>T XP_011519450.1:p.Gly730Cys
NM_005477.3:c.3406G>T MANE Select NP_005468.1:p.Gly1136Cys
Search 100 bp 5'
Search 100 bp 3'