Canonical Allele Identifier: CA491478346
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615698C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323357C>T , CM000677.2:g.73323357C>T GRCh38
NC_000015.9:g.73615698C>T , CM000677.1:g.73615698C>T GRCh37
NC_000015.8:g.71402751C>T NCBI36
NG_009063.1:g.50908G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2736G>A MANE Select ENSP00000261917.3:p.Lys912=
ENST00000261917.3:c.2736G>A ENSP00000261917.3:p.Lys912=
NM_005477.2:c.2736G>A NP_005468.1:p.Lys912=
XM_011521148.1:c.1518G>A XP_011519450.1:p.Lys506=
XM_011521148.2:c.1518G>A XP_011519450.1:p.Lys506=
NM_005477.3:c.2736G>A MANE Select NP_005468.1:p.Lys912=