Canonical Allele Identifier: CA2629370937
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73324039-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324039T>A , CM000677.2:g.73324039T>A GRCh38
NC_000015.9:g.73616380T>A , CM000677.1:g.73616380T>A GRCh37
NC_000015.8:g.71403433T>A NCBI36
NG_009063.1:g.50226A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2143+50A>T MANE Select ENSP00000261917.3:n.2143+50A>T
ENST00000261917.3:c.2143+50A>T ENSP00000261917.3:n.2143+50A>T
NM_005477.2:c.2143+50A>T NP_005468.1:n.2143+50A>T
XM_011521148.1:c.925+50A>T XP_011519450.1:n.925+50A>T
XM_011521148.2:c.925+50A>T XP_011519450.1:n.925+50A>T
NM_005477.3:c.2143+50A>T MANE Select NP_005468.1:n.2143+50A>T
Search 100 bp 5'
Search 100 bp 3'