Canonical Allele Identifier: CA491478008

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322937-C-T
• MyVariant Identifiers: chr15:g.73615278C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322937C>T , CM000677.2:g.73322937C>T	GRCh38
NC_000015.9:g.73615278C>T , CM000677.1:g.73615278C>T	GRCh37
NC_000015.8:g.71402331C>T	NCBI36
NG_009063.1:g.51328G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3156G>A MANE Select	ENSP00000261917.3:p.Leu1052=
ENST00000261917.3:c.3156G>A	ENSP00000261917.3:p.Leu1052=
NM_005477.2:c.3156G>A	NP_005468.1:p.Leu1052=
XM_011521148.1:c.1938G>A	XP_011519450.1:p.Leu646=
XM_011521148.2:c.1938G>A	XP_011519450.1:p.Leu646=
NM_005477.3:c.3156G>A MANE Select	NP_005468.1:p.Leu1052=