Canonical Allele Identifier: CA2187187298

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323034G= , CM000677.2:g.73323034G=	GRCh38
NC_000015.9:g.73615375G= , CM000677.1:g.73615375G=	GRCh37
NC_000015.8:g.71402428G=	NCBI36
NG_009063.1:g.51231C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3059C= MANE Select	ENSP00000261917.3:p.Thr1020=
ENST00000261917.3:c.3059C=	ENSP00000261917.3:p.Thr1020=
NM_005477.2:c.3059C=	NP_005468.1:p.Thr1020=
XM_011521148.1:c.1841C=	XP_011519450.1:p.Thr614=
XM_011521148.2:c.1841C=	XP_011519450.1:p.Thr614=
NM_005477.3:c.3059C= MANE Select	NP_005468.1:p.Thr1020=