Canonical Allele Identifier: CA2187187882

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323272G= , CM000677.2:g.73323272G=	GRCh38
NC_000015.9:g.73615613G= , CM000677.1:g.73615613G=	GRCh37
NC_000015.8:g.71402666G=	NCBI36
NG_009063.1:g.50993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2821C= MANE Select	ENSP00000261917.3:p.Pro941=
ENST00000261917.3:c.2821C=	ENSP00000261917.3:p.Pro941=
NM_005477.2:c.2821C=	NP_005468.1:p.Pro941=
XM_011521148.1:c.1603C=	XP_011519450.1:p.Pro535=
XM_011521148.2:c.1603C=	XP_011519450.1:p.Pro535=
NM_005477.3:c.2821C= MANE Select	NP_005468.1:p.Pro941=