Canonical Allele Identifier: CA222867

Gene: HCN4

Linked Data

• ClinVar Variation Id: 95283
• ClinVar RCV Id: RCV000081297 ; RCV000723657 ; RCV001085378
• dbSNP Id: rs200303699
• ExAC: 15:73624463 C / T
• gnomAD v2: 15-73624463-C-T
• gnomAD v3: 15-73332122-C-T
• gnomAD v4: 15-73332122-C-T
• MyVariant Identifiers: chr15:g.73624463C>T (hg19) ; chr15:g.73332122C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332122C>T , CM000677.2:g.73332122C>T	GRCh38
NC_000015.9:g.73624463C>T , CM000677.1:g.73624463C>T	GRCh37
NC_000015.8:g.71411516C>T	NCBI36
NG_009063.1:g.42143G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1371+9G>A MANE Select	ENSP00000261917.3:n.1371+9G>A
ENST00000261917.3:c.1371+9G>A	ENSP00000261917.3:n.1371+9G>A
NM_005477.2:c.1371+9G>A	NP_005468.1:n.1371+9G>A
XM_011521148.1:c.153+9G>A	XP_011519450.1:n.153+9G>A
XM_011521148.2:c.153+9G>A	XP_011519450.1:n.153+9G>A
NM_005477.3:c.1371+9G>A MANE Select	NP_005468.1:n.1371+9G>A