Canonical Allele Identifier: CA504875818
Gene: HCN2 HGNC NCBI

Linked Data

gnomAD v4: 19-615979-G-C
MyVariant Identifiers: chr19:g.615979G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615979G>C , CM000681.2:g.615979G>C GRCh38
NC_000019.9:g.615979G>C , CM000681.1:g.615979G>C GRCh37
NC_000019.8:g.566979G>C NCBI36
NG_023049.1:g.22590C>G
NG_052810.1:g.31087G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2175G>C MANE Select ENSP00000251287.1:p.Ser725=
ENST00000251287.2:c.2175G>C ENSP00000251287.1:p.Ser725=
NM_001194.3:c.2175G>C NP_001185.3:p.Ser725=
NM_001194.4:c.2175G>C MANE Select NP_001185.3:p.Ser725=
Search 100 bp 5'
Search 100 bp 3'