Canonical Allele Identifier: CA402887027
Gene: HCN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.615992C>A (hg19) chr19:g.615992C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615992C>A , CM000681.2:g.615992C>A GRCh38
NC_000019.9:g.615992C>A , CM000681.1:g.615992C>A GRCh37
NC_000019.8:g.566992C>A NCBI36
NG_023049.1:g.22577G>T
NG_052810.1:g.31100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2188C>A MANE Select ENSP00000251287.1:p.Leu730Met
ENST00000251287.2:c.2188C>A ENSP00000251287.1:p.Leu730Met
NM_001194.3:c.2188C>A NP_001185.3:p.Leu730Met
NM_001194.4:c.2188C>A MANE Select NP_001185.3:p.Leu730Met
Search 100 bp 5'
Search 100 bp 3'