Canonical Allele Identifier: CA272662892
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs537252175
gnomAD v3: 15-73322396-T-A
gnomAD v4: 15-73322396-T-A
MyVariant Identifiers: chr15:g.73614737T>A (hg19) chr15:g.73322396T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322396T>A , CM000677.2:g.73322396T>A GRCh38
NC_000015.9:g.73614737T>A , CM000677.1:g.73614737T>A GRCh37
NC_000015.8:g.71401790T>A NCBI36
NG_009063.1:g.51869A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*85A>T MANE Select ENSP00000261917.3:n.*85A>T
ENST00000261917.3:c.*85A>T ENSP00000261917.3:n.*85A>T
NM_005477.2:c.*85A>T NP_005468.1:n.*85A>T
XM_011521148.1:c.*85A>T XP_011519450.1:n.*85A>T
XM_011521148.2:c.*85A>T XP_011519450.1:n.*85A>T
NM_005477.3:c.*85A>T MANE Select NP_005468.1:n.*85A>T
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