Canonical Allele Identifier: CA491478440

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615407C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323066C>T , CM000677.2:g.73323066C>T	GRCh38
NC_000015.9:g.73615407C>T , CM000677.1:g.73615407C>T	GRCh37
NC_000015.8:g.71402460C>T	NCBI36
NG_009063.1:g.51199G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3027G>A MANE Select	ENSP00000261917.3:p.Gly1009=
ENST00000261917.3:c.3027G>A	ENSP00000261917.3:p.Gly1009=
NM_005477.2:c.3027G>A	NP_005468.1:p.Gly1009=
XM_011521148.1:c.1809G>A	XP_011519450.1:p.Gly603=
XM_011521148.2:c.1809G>A	XP_011519450.1:p.Gly603=
NM_005477.3:c.3027G>A MANE Select	NP_005468.1:p.Gly1009=