Canonical Allele Identifier: CA2187169619

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332068G= , CM000677.2:g.73332068G=	GRCh38
NC_000015.9:g.73624409G= , CM000677.1:g.73624409G=	GRCh37
NC_000015.8:g.71411462G=	NCBI36
NG_009063.1:g.42197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1371+63C= MANE Select	ENSP00000261917.3:n.1371+63C=
ENST00000261917.3:c.1371+63C=	ENSP00000261917.3:n.1371+63C=
NM_005477.2:c.1371+63C=	NP_005468.1:n.1371+63C=
XM_011521148.1:c.153+63C=	XP_011519450.1:n.153+63C=
XM_011521148.2:c.153+63C=	XP_011519450.1:n.153+63C=
NM_005477.3:c.1371+63C= MANE Select	NP_005468.1:n.1371+63C=