Canonical Allele Identifier: CA272665111
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs917722202
gnomAD v2: 15-73616228-A-G
gnomAD v4: 15-73323887-A-G
MyVariant Identifiers: chr15:g.73616228A>G (hg19) chr15:g.73323887A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323887A>G , CM000677.2:g.73323887A>G GRCh38
NC_000015.9:g.73616228A>G , CM000677.1:g.73616228A>G GRCh37
NC_000015.8:g.71403281A>G NCBI36
NG_009063.1:g.50378T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2206T>C MANE Select ENSP00000261917.3:p.Tyr736His
ENST00000261917.3:c.2206T>C ENSP00000261917.3:p.Tyr736His
NM_005477.2:c.2206T>C NP_005468.1:p.Tyr736His
XM_011521148.1:c.988T>C XP_011519450.1:p.Tyr330His
XM_011521148.2:c.988T>C XP_011519450.1:p.Tyr330His
NM_005477.3:c.2206T>C MANE Select NP_005468.1:p.Tyr736His
Search 100 bp 5'
Search 100 bp 3'