Canonical Allele Identifier: CA491477914
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615227C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322886C>T , CM000677.2:g.73322886C>T GRCh38
NC_000015.9:g.73615227C>T , CM000677.1:g.73615227C>T GRCh37
NC_000015.8:g.71402280C>T NCBI36
NG_009063.1:g.51379G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3207G>A MANE Select ENSP00000261917.3:p.Arg1069=
ENST00000261917.3:c.3207G>A ENSP00000261917.3:p.Arg1069=
NM_005477.2:c.3207G>A NP_005468.1:p.Arg1069=
XM_011521148.1:c.1989G>A XP_011519450.1:p.Arg663=
XM_011521148.2:c.1989G>A XP_011519450.1:p.Arg663=
NM_005477.3:c.3207G>A MANE Select NP_005468.1:p.Arg1069=