Canonical Allele Identifier: CA491478555
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616061C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323720C>T , CM000677.2:g.73323720C>T GRCh38
NC_000015.9:g.73616061C>T , CM000677.1:g.73616061C>T GRCh37
NC_000015.8:g.71403114C>T NCBI36
NG_009063.1:g.50545G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2373G>A MANE Select ENSP00000261917.3:p.Val791=
ENST00000261917.3:c.2373G>A ENSP00000261917.3:p.Val791=
NM_005477.2:c.2373G>A NP_005468.1:p.Val791=
XM_011521148.1:c.1155G>A XP_011519450.1:p.Val385=
XM_011521148.2:c.1155G>A XP_011519450.1:p.Val385=
NM_005477.3:c.2373G>A MANE Select NP_005468.1:p.Val791=
Search 100 bp 5'
Search 100 bp 3'