Canonical Allele Identifier: CA491478669

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323891-G-A
• MyVariant Identifiers: chr15:g.73616232G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323891G>A , CM000677.2:g.73323891G>A	GRCh38
NC_000015.9:g.73616232G>A , CM000677.1:g.73616232G>A	GRCh37
NC_000015.8:g.71403285G>A	NCBI36
NG_009063.1:g.50374C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2202C>T MANE Select	ENSP00000261917.3:p.Phe734=
ENST00000261917.3:c.2202C>T	ENSP00000261917.3:p.Phe734=
NM_005477.2:c.2202C>T	NP_005468.1:p.Phe734=
XM_011521148.1:c.984C>T	XP_011519450.1:p.Phe328=
XM_011521148.2:c.984C>T	XP_011519450.1:p.Phe328=
NM_005477.3:c.2202C>T MANE Select	NP_005468.1:p.Phe734=