Canonical Allele Identifier: CA2187188617

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323713C= , CM000677.2:g.73323713C=	GRCh38
NC_000015.9:g.73616054C= , CM000677.1:g.73616054C=	GRCh37
NC_000015.8:g.71403107C=	NCBI36
NG_009063.1:g.50552G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2380G= MANE Select	ENSP00000261917.3:p.Ala794=
ENST00000261917.3:c.2380G=	ENSP00000261917.3:p.Ala794=
NM_005477.2:c.2380G=	NP_005468.1:p.Ala794=
XM_011521148.1:c.1162G=	XP_011519450.1:p.Ala388=
XM_011521148.2:c.1162G=	XP_011519450.1:p.Ala388=
NM_005477.3:c.2380G= MANE Select	NP_005468.1:p.Ala794=