Canonical Allele Identifier: CA2187188620

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323719C= , CM000677.2:g.73323719C=	GRCh38
NC_000015.9:g.73616060C= , CM000677.1:g.73616060C=	GRCh37
NC_000015.8:g.71403113C=	NCBI36
NG_009063.1:g.50546G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2374G= MANE Select	ENSP00000261917.3:p.Ala792=
ENST00000261917.3:c.2374G=	ENSP00000261917.3:p.Ala792=
NM_005477.2:c.2374G=	NP_005468.1:p.Ala792=
XM_011521148.1:c.1156G=	XP_011519450.1:p.Ala386=
XM_011521148.2:c.1156G=	XP_011519450.1:p.Ala386=
NM_005477.3:c.2374G= MANE Select	NP_005468.1:p.Ala792=