Canonical Allele Identifier: CA491479283
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367839-C-A
MyVariant Identifiers: chr15:g.73660180C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367839C>A , CM000677.2:g.73367839C>A GRCh38
NC_000015.9:g.73660180C>A , CM000677.1:g.73660180C>A GRCh37
NC_000015.8:g.71447233C>A NCBI36
NG_009063.1:g.6426G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.432G>T MANE Select ENSP00000261917.3:p.Thr144=
ENST00000261917.3:c.432G>T ENSP00000261917.3:p.Thr144=
NM_005477.2:c.432G>T NP_005468.1:p.Thr144=
NM_005477.3:c.432G>T MANE Select NP_005468.1:p.Thr144=
Search 100 bp 5'
Search 100 bp 3'