Canonical Allele Identifier: CA504875689
Gene: HCN2 HGNC NCBI

Linked Data

dbSNP Id: rs1983885791
gnomAD v3: 19-615913-G-A
gnomAD v4: 19-615913-G-A
MyVariant Identifiers: chr19:g.615913G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615913G>A , CM000681.2:g.615913G>A GRCh38
NC_000019.9:g.615913G>A , CM000681.1:g.615913G>A GRCh37
NC_000019.8:g.566913G>A NCBI36
NG_023049.1:g.22656C>T
NG_052810.1:g.31021G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2109G>A MANE Select ENSP00000251287.1:p.Gln703=
ENST00000251287.2:c.2109G>A ENSP00000251287.1:p.Gln703=
NM_001194.3:c.2109G>A NP_001185.3:p.Gln703=
NM_001194.4:c.2109G>A MANE Select NP_001185.3:p.Gln703=
Search 100 bp 5'
Search 100 bp 3'