Canonical Allele Identifier: CA393098468
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367981-C-A
MyVariant Identifiers: chr15:g.73660322C>A (hg19) chr15:g.73367981C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367981C>A , CM000677.2:g.73367981C>A GRCh38
NC_000015.9:g.73660322C>A , CM000677.1:g.73660322C>A GRCh37
NC_000015.8:g.71447375C>A NCBI36
NG_009063.1:g.6284G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.290G>T MANE Select ENSP00000261917.3:p.Arg97Leu
ENST00000261917.3:c.290G>T ENSP00000261917.3:p.Arg97Leu
NM_005477.2:c.290G>T NP_005468.1:p.Arg97Leu
NM_005477.3:c.290G>T MANE Select NP_005468.1:p.Arg97Leu
Search 100 bp 5'
Search 100 bp 3'