Canonical Allele Identifier: CA2187188189

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323392C= , CM000677.2:g.73323392C=	GRCh38
NC_000015.9:g.73615733C= , CM000677.1:g.73615733C=	GRCh37
NC_000015.8:g.71402786C=	NCBI36
NG_009063.1:g.50873G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2701G= MANE Select	ENSP00000261917.3:p.Ala901=
ENST00000261917.3:c.2701G=	ENSP00000261917.3:p.Ala901=
NM_005477.2:c.2701G=	NP_005468.1:p.Ala901=
XM_011521148.1:c.1483G=	XP_011519450.1:p.Ala495=
XM_011521148.2:c.1483G=	XP_011519450.1:p.Ala495=
NM_005477.3:c.2701G= MANE Select	NP_005468.1:p.Ala901=