Canonical Allele Identifier: CA2587753788
Gene: HCN2 HGNC NCBI

Linked Data

gnomAD v4: 19-615966-CGCA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615968_615970del , CM000681.2:g.615968_615970del GRCh38
NC_000019.9:g.615968_615970del , CM000681.1:g.615968_615970del GRCh37
NC_000019.8:g.566968_566970del NCBI36
NG_023049.1:g.22600_22602del
NG_052810.1:g.31076_31078del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2164_2166del MANE Select ENSP00000251287.1:p.Gln722del
ENST00000251287.2:c.2164_2166del ENSP00000251287.1:p.Gln722del
NM_001194.3:c.2164_2166del NP_001185.3:p.Gln722del
NM_001194.4:c.2164_2166del MANE Select NP_001185.3:p.Gln722del
Search 100 bp 5'
Search 100 bp 3'