Canonical Allele Identifier: CA491478310

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323029-G-T
• MyVariant Identifiers: chr15:g.73615370G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323029G>T , CM000677.2:g.73323029G>T	GRCh38
NC_000015.9:g.73615370G>T , CM000677.1:g.73615370G>T	GRCh37
NC_000015.8:g.71402423G>T	NCBI36
NG_009063.1:g.51236C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3064C>A MANE Select	ENSP00000261917.3:p.Arg1022=
ENST00000261917.3:c.3064C>A	ENSP00000261917.3:p.Arg1022=
NM_005477.2:c.3064C>A	NP_005468.1:p.Arg1022=
XM_011521148.1:c.1846C>A	XP_011519450.1:p.Arg616=
XM_011521148.2:c.1846C>A	XP_011519450.1:p.Arg616=
NM_005477.3:c.3064C>A MANE Select	NP_005468.1:p.Arg1022=