Canonical Allele Identifier: CA491151482

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73621971G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329630G>C , CM000677.2:g.73329630G>C	GRCh38
NC_000015.9:g.73621971G>C , CM000677.1:g.73621971G>C	GRCh37
NC_000015.8:g.71409024G>C	NCBI36
NG_009063.1:g.44635C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1533C>G MANE Select	ENSP00000261917.3:p.Gly511=
ENST00000261917.3:c.1533C>G	ENSP00000261917.3:p.Gly511=
NM_005477.2:c.1533C>G	NP_005468.1:p.Gly511=
XM_011521148.1:c.315C>G	XP_011519450.1:p.Gly105=
XM_011521148.2:c.315C>G	XP_011519450.1:p.Gly105=
NM_005477.3:c.1533C>G MANE Select	NP_005468.1:p.Gly511=