Canonical Allele Identifier: CA2317211290

Gene: HCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.613942A= , CM000681.2:g.613942A=	GRCh38
NC_000019.9:g.613942A= , CM000681.1:g.613942A=	GRCh37
NC_000019.8:g.564942A=	NCBI36
NG_052810.1:g.29050A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251287.3:c.1916A= MANE Select	ENSP00000251287.1:p.Asn639=
ENST00000251287.2:c.1916A=	ENSP00000251287.1:p.Asn639=
NM_001194.3:c.1916A=	NP_001185.3:p.Asn639=
NM_001194.4:c.1916A= MANE Select	NP_001185.3:p.Asn639=