Canonical Allele Identifier: CA491478154
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615077G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322736G>A , CM000677.2:g.73322736G>A GRCh38
NC_000015.9:g.73615077G>A , CM000677.1:g.73615077G>A GRCh37
NC_000015.8:g.71402130G>A NCBI36
NG_009063.1:g.51529C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3357C>T MANE Select ENSP00000261917.3:p.Phe1119=
ENST00000261917.3:c.3357C>T ENSP00000261917.3:p.Phe1119=
NM_005477.2:c.3357C>T NP_005468.1:p.Phe1119=
XM_011521148.1:c.2139C>T XP_011519450.1:p.Phe713=
XM_011521148.2:c.2139C>T XP_011519450.1:p.Phe713=
NM_005477.3:c.3357C>T MANE Select NP_005468.1:p.Phe1119=