Canonical Allele Identifier: CA631293049
Gene: HCN2 HGNC NCBI

Linked Data

dbSNP Id: rs1243812656
gnomAD v2: 19-615962-C-CCTT
gnomAD v4: 19-615962-C-CCTT
MyVariant Identifiers: chr19:g.615962_615963insCTT (hg19) chr19:g.615962_615963insCTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615963_615964insTTC , CM000681.2:g.615963_615964insTTC GRCh38
NC_000019.9:g.615963_615964insTTC , CM000681.1:g.615963_615964insTTC GRCh37
NC_000019.8:g.566963_566964insTTC NCBI36
NG_023049.1:g.22606_22607insAAG
NG_052810.1:g.31071_31072insTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2159_2160insTTC MANE Select ENSP00000251287.1:p.Pro720_Pro721insSer
ENST00000251287.2:c.2159_2160insTTC ENSP00000251287.1:p.Pro720_Pro721insSer
NM_001194.3:c.2159_2160insTTC NP_001185.3:p.Pro720_Pro721insSer
NM_001194.4:c.2159_2160insTTC MANE Select NP_001185.3:p.Pro720_Pro721insSer
Search 100 bp 5'
Search 100 bp 3'