Canonical Allele Identifier: CA393084800
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1476366158
gnomAD v2: 15-73614868-C-T
MyVariant Identifiers: chr15:g.73614868C>T (hg19) chr15:g.73322527C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322527C>T , CM000677.2:g.73322527C>T GRCh38
NC_000015.9:g.73614868C>T , CM000677.1:g.73614868C>T GRCh37
NC_000015.8:g.71401921C>T NCBI36
NG_009063.1:g.51738G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3566G>A MANE Select ENSP00000261917.3:p.Gly1189Glu
ENST00000261917.3:c.3566G>A ENSP00000261917.3:p.Gly1189Glu
NM_005477.2:c.3566G>A NP_005468.1:p.Gly1189Glu
XM_011521148.1:c.2348G>A XP_011519450.1:p.Gly783Glu
XM_011521148.2:c.2348G>A XP_011519450.1:p.Gly783Glu
NM_005477.3:c.3566G>A MANE Select NP_005468.1:p.Gly1189Glu
Search 100 bp 5'
Search 100 bp 3'