Canonical Allele Identifier: CA491478045

Gene: HCN4

Linked Data

• ClinVar Variation Id: 799787
• ClinVar RCV Id: RCV000983406 ; RCV002320197
• dbSNP Id: rs1342751732
• gnomAD v2: 15-73615299-G-A
• gnomAD v3: 15-73322958-G-A
• gnomAD v4: 15-73322958-G-A
• MyVariant Identifiers: chr15:g.73615299G>A (hg19) ; chr15:g.73322958G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322958G>A , CM000677.2:g.73322958G>A	GRCh38
NC_000015.9:g.73615299G>A , CM000677.1:g.73615299G>A	GRCh37
NC_000015.8:g.71402352G>A	NCBI36
NG_009063.1:g.51307C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3135C>T MANE Select	ENSP00000261917.3:p.Ala1045=
ENST00000261917.3:c.3135C>T	ENSP00000261917.3:p.Ala1045=
NM_005477.2:c.3135C>T	NP_005468.1:p.Ala1045=
XM_011521148.1:c.1917C>T	XP_011519450.1:p.Ala639=
XM_011521148.2:c.1917C>T	XP_011519450.1:p.Ala639=
NM_005477.3:c.3135C>T MANE Select	NP_005468.1:p.Ala1045=