Canonical Allele Identifier: CA393086015
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2963898
ClinVar RCV Id: RCV003825536
dbSNP Id: rs776270218
gnomAD v2: 15-73615231-C-G
MyVariant Identifiers: chr15:g.73615231C>G (hg19) chr15:g.73322890C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322890C>G , CM000677.2:g.73322890C>G GRCh38
NC_000015.9:g.73615231C>G , CM000677.1:g.73615231C>G GRCh37
NC_000015.8:g.71402284C>G NCBI36
NG_009063.1:g.51375G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3203G>C MANE Select ENSP00000261917.3:p.Arg1068Pro
ENST00000261917.3:c.3203G>C ENSP00000261917.3:p.Arg1068Pro
NM_005477.2:c.3203G>C NP_005468.1:p.Arg1068Pro
XM_011521148.1:c.1985G>C XP_011519450.1:p.Arg662Pro
XM_011521148.2:c.1985G>C XP_011519450.1:p.Arg662Pro
NM_005477.3:c.3203G>C MANE Select NP_005468.1:p.Arg1068Pro
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