Canonical Allele Identifier: CA491478142

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615062A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322721A>G , CM000677.2:g.73322721A>G	GRCh38
NC_000015.9:g.73615062A>G , CM000677.1:g.73615062A>G	GRCh37
NC_000015.8:g.71402115A>G	NCBI36
NG_009063.1:g.51544T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3372T>C MANE Select	ENSP00000261917.3:p.Gly1124=
ENST00000261917.3:c.3372T>C	ENSP00000261917.3:p.Gly1124=
NM_005477.2:c.3372T>C	NP_005468.1:p.Gly1124=
XM_011521148.1:c.2154T>C	XP_011519450.1:p.Gly718=
XM_011521148.2:c.2154T>C	XP_011519450.1:p.Gly718=
NM_005477.3:c.3372T>C MANE Select	NP_005468.1:p.Gly1124=