Canonical Allele Identifier: CA14086101

Gene: HCN4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73359833A>G , CM000677.2:g.73359833A>G	GRCh38
NC_000015.9:g.73652174A>G , CM000677.1:g.73652174A>G	GRCh37
NC_000015.8:g.71439227A>G	NCBI36
NG_009063.1:g.14432T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.785+7653T>C MANE Select	ENSP00000261917.3:n.785+7653T>C
ENST00000261917.3:c.785+7653T>C	ENSP00000261917.3:n.785+7653T>C
NM_005477.2:c.785+7653T>C	NP_005468.1:n.785+7653T>C
NM_005477.3:c.785+7653T>C MANE Select	NP_005468.1:n.785+7653T>C