Canonical Allele Identifier: CA491478326

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615374A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323033A>C , CM000677.2:g.73323033A>C	GRCh38
NC_000015.9:g.73615374A>C , CM000677.1:g.73615374A>C	GRCh37
NC_000015.8:g.71402427A>C	NCBI36
NG_009063.1:g.51232T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3060T>G MANE Select	ENSP00000261917.3:p.Thr1020=
ENST00000261917.3:c.3060T>G	ENSP00000261917.3:p.Thr1020=
NM_005477.2:c.3060T>G	NP_005468.1:p.Thr1020=
XM_011521148.1:c.1842T>G	XP_011519450.1:p.Thr614=
XM_011521148.2:c.1842T>G	XP_011519450.1:p.Thr614=
NM_005477.3:c.3060T>G MANE Select	NP_005468.1:p.Thr1020=