Canonical Allele Identifier: CA402886959

Gene: HCN2

Linked Data

• MyVariant Identifiers: chr19:g.615980G>T (hg19) ; chr19:g.615980G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.615980G>T , CM000681.2:g.615980G>T	GRCh38
NC_000019.9:g.615980G>T , CM000681.1:g.615980G>T	GRCh37
NC_000019.8:g.566980G>T	NCBI36
NG_023049.1:g.22589C>A
NG_052810.1:g.31088G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251287.3:c.2176G>T MANE Select	ENSP00000251287.1:p.Ala726Ser
ENST00000251287.2:c.2176G>T	ENSP00000251287.1:p.Ala726Ser
NM_001194.3:c.2176G>T	NP_001185.3:p.Ala726Ser
NM_001194.4:c.2176G>T MANE Select	NP_001185.3:p.Ala726Ser