Canonical Allele Identifier: CA491478863

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615866G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323525G>T , CM000677.2:g.73323525G>T	GRCh38
NC_000015.9:g.73615866G>T , CM000677.1:g.73615866G>T	GRCh37
NC_000015.8:g.71402919G>T	NCBI36
NG_009063.1:g.50740C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2568C>A MANE Select	ENSP00000261917.3:p.Ser856=
ENST00000261917.3:c.2568C>A	ENSP00000261917.3:p.Ser856=
NM_005477.2:c.2568C>A	NP_005468.1:p.Ser856=
XM_011521148.1:c.1350C>A	XP_011519450.1:p.Ser450=
XM_011521148.2:c.1350C>A	XP_011519450.1:p.Ser450=
NM_005477.3:c.2568C>A MANE Select	NP_005468.1:p.Ser856=