Canonical Allele Identifier: CA491477767

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615110G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322769G>C , CM000677.2:g.73322769G>C	GRCh38
NC_000015.9:g.73615110G>C , CM000677.1:g.73615110G>C	GRCh37
NC_000015.8:g.71402163G>C	NCBI36
NG_009063.1:g.51496C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3324C>G MANE Select	ENSP00000261917.3:p.Ser1108=
ENST00000261917.3:c.3324C>G	ENSP00000261917.3:p.Ser1108=
NM_005477.2:c.3324C>G	NP_005468.1:p.Ser1108=
XM_011521148.1:c.2106C>G	XP_011519450.1:p.Ser702=
XM_011521148.2:c.2106C>G	XP_011519450.1:p.Ser702=
NM_005477.3:c.3324C>G MANE Select	NP_005468.1:p.Ser1108=