Canonical Allele Identifier: CA2317212814
Gene: HCN2 HGNC NCBI
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2176G= MANE Select ENSP00000251287.1:p.Ala726=
ENST00000251287.2:c.2176G= ENSP00000251287.1:p.Ala726=
NM_001194.3:c.2176G= NP_001185.3:p.Ala726=
NM_001194.4:c.2176G= MANE Select NP_001185.3:p.Ala726=
Search 100 bp 5'
Search 100 bp 3'