Canonical Allele Identifier: CA2187167618

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329720G= , CM000677.2:g.73329720G=	GRCh38
NC_000015.9:g.73622061G= , CM000677.1:g.73622061G=	GRCh37
NC_000015.8:g.71409114G=	NCBI36
NG_009063.1:g.44545C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1443C= MANE Select	ENSP00000261917.3:p.Tyr481=
ENST00000261917.3:c.1443C=	ENSP00000261917.3:p.Tyr481=
NM_005477.2:c.1443C=	NP_005468.1:p.Tyr481=
XM_011521148.1:c.225C=	XP_011519450.1:p.Tyr75=
XM_011521148.2:c.225C=	XP_011519450.1:p.Tyr75=
NM_005477.3:c.1443C= MANE Select	NP_005468.1:p.Tyr481=