Canonical Allele Identifier: CA9018881

Gene: HCN2

Linked Data

• dbSNP Id: rs765394313
• ExAC: 19:616024 G / A
• gnomAD v2: 19-616024-G-A
• gnomAD v3: 19-616024-G-A
• gnomAD v4: 19-616024-G-A
• MyVariant Identifiers: chr19:g.616024G>A (hg19) ; chr19:g.616024G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.616024G>A , CM000681.2:g.616024G>A	GRCh38
NC_000019.9:g.616024G>A , CM000681.1:g.616024G>A	GRCh37
NC_000019.8:g.567024G>A	NCBI36
NG_023049.1:g.22545C>T
NG_052810.1:g.31132G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251287.3:c.2220G>A MANE Select	ENSP00000251287.1:p.Pro740=
ENST00000251287.2:c.2220G>A	ENSP00000251287.1:p.Pro740=
NM_001194.3:c.2220G>A	NP_001185.3:p.Pro740=
NM_001194.4:c.2220G>A MANE Select	NP_001185.3:p.Pro740=