Canonical Allele Identifier: CA2187188324

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323455A= , CM000677.2:g.73323455A=	GRCh38
NC_000015.9:g.73615796A= , CM000677.1:g.73615796A=	GRCh37
NC_000015.8:g.71402849A=	NCBI36
NG_009063.1:g.50810T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2638T= MANE Select	ENSP00000261917.3:p.Ser880=
ENST00000261917.3:c.2638T=	ENSP00000261917.3:p.Ser880=
NM_005477.2:c.2638T=	NP_005468.1:p.Ser880=
XM_011521148.1:c.1420T=	XP_011519450.1:p.Ser474=
XM_011521148.2:c.1420T=	XP_011519450.1:p.Ser474=
NM_005477.3:c.2638T= MANE Select	NP_005468.1:p.Ser880=