Canonical Allele Identifier: CA2187167513

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329677T= , CM000677.2:g.73329677T=	GRCh38
NC_000015.9:g.73622018T= , CM000677.1:g.73622018T=	GRCh37
NC_000015.8:g.71409071T=	NCBI36
NG_009063.1:g.44588A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1486A= MANE Select	ENSP00000261917.3:p.Met496=
ENST00000261917.3:c.1486A=	ENSP00000261917.3:p.Met496=
NM_005477.2:c.1486A=	NP_005468.1:p.Met496=
XM_011521148.1:c.268A=	XP_011519450.1:p.Met90=
XM_011521148.2:c.268A=	XP_011519450.1:p.Met90=
NM_005477.3:c.1486A= MANE Select	NP_005468.1:p.Met496=