Canonical Allele Identifier: CA2518988052

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332028T>A , CM000677.2:g.73332028T>A	GRCh38
NC_000015.9:g.73624369T>A , CM000677.1:g.73624369T>A	GRCh37
NC_000015.8:g.71411422T>A	NCBI36
NG_009063.1:g.42237A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1371+103A>T MANE Select	ENSP00000261917.3:n.1371+103A>T
ENST00000261917.3:c.1371+103A>T	ENSP00000261917.3:n.1371+103A>T
NM_005477.2:c.1371+103A>T	NP_005468.1:n.1371+103A>T
XM_011521148.1:c.153+103A>T	XP_011519450.1:n.153+103A>T
XM_011521148.2:c.153+103A>T	XP_011519450.1:n.153+103A>T
NM_005477.3:c.1371+103A>T MANE Select	NP_005468.1:n.1371+103A>T