Canonical Allele Identifier: CA2187169610

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332056A= , CM000677.2:g.73332056A=	GRCh38
NC_000015.9:g.73624397A= , CM000677.1:g.73624397A=	GRCh37
NC_000015.8:g.71411450A=	NCBI36
NG_009063.1:g.42209T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1371+75T= MANE Select	ENSP00000261917.3:n.1371+75T=
ENST00000261917.3:c.1371+75T=	ENSP00000261917.3:n.1371+75T=
NM_005477.2:c.1371+75T=	NP_005468.1:n.1371+75T=
XM_011521148.1:c.153+75T=	XP_011519450.1:n.153+75T=
XM_011521148.2:c.153+75T=	XP_011519450.1:n.153+75T=
NM_005477.3:c.1371+75T= MANE Select	NP_005468.1:n.1371+75T=