Canonical Allele Identifier: CA272663408

Gene: HCN4

Linked Data

• ClinVar Variation Id: 1354312
• ClinVar RCV Id: RCV001887782 ; RCV002458659
• dbSNP Id: rs940405280
• gnomAD v2: 15-73615117-G-A
• gnomAD v3: 15-73322776-G-A
• gnomAD v4: 15-73322776-G-A
• MyVariant Identifiers: chr15:g.73615117G>A (hg19) ; chr15:g.73322776G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322776G>A , CM000677.2:g.73322776G>A	GRCh38
NC_000015.9:g.73615117G>A , CM000677.1:g.73615117G>A	GRCh37
NC_000015.8:g.71402170G>A	NCBI36
NG_009063.1:g.51489C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3317C>T MANE Select	ENSP00000261917.3:p.Pro1106Leu
ENST00000261917.3:c.3317C>T	ENSP00000261917.3:p.Pro1106Leu
NM_005477.2:c.3317C>T	NP_005468.1:p.Pro1106Leu
XM_011521148.1:c.2099C>T	XP_011519450.1:p.Pro700Leu
XM_011521148.2:c.2099C>T	XP_011519450.1:p.Pro700Leu
NM_005477.3:c.3317C>T MANE Select	NP_005468.1:p.Pro1106Leu