Canonical Allele Identifier: CA491478584

Gene: HCN4

Linked Data

• ClinVar Variation Id: 3004639
• ClinVar RCV Id: RCV003860742
• MyVariant Identifiers: chr15:g.73615455C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323114C>G , CM000677.2:g.73323114C>G	GRCh38
NC_000015.9:g.73615455C>G , CM000677.1:g.73615455C>G	GRCh37
NC_000015.8:g.71402508C>G	NCBI36
NG_009063.1:g.51151G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2979G>C MANE Select	ENSP00000261917.3:p.Thr993=
ENST00000261917.3:c.2979G>C	ENSP00000261917.3:p.Thr993=
NM_005477.2:c.2979G>C	NP_005468.1:p.Thr993=
XM_011521148.1:c.1761G>C	XP_011519450.1:p.Thr587=
XM_011521148.2:c.1761G>C	XP_011519450.1:p.Thr587=
NM_005477.3:c.2979G>C MANE Select	NP_005468.1:p.Thr993=