Canonical Allele Identifier: CA619410666
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1413620108
gnomAD v2: 15-73621865-C-CT
gnomAD v3: 15-73329524-C-CT
gnomAD v4: 15-73329524-C-CT
MyVariant Identifiers: chr15:g.73621865_73621866insT (hg19) chr15:g.73329524_73329525insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329525dup , CM000677.2:g.73329525dup GRCh38
NC_000015.9:g.73621866dup , CM000677.1:g.73621866dup GRCh37
NC_000015.8:g.71408919dup NCBI36
NG_009063.1:g.44740dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1590+48dup MANE Select ENSP00000261917.3:n.1590+48dup
ENST00000261917.3:c.1590+48dup ENSP00000261917.3:n.1590+48dup
NM_005477.2:c.1590+48dup NP_005468.1:n.1590+48dup
XM_011521148.1:c.372+48dup XP_011519450.1:n.372+48dup
XM_011521148.2:c.372+48dup XP_011519450.1:n.372+48dup
NM_005477.3:c.1590+48dup MANE Select NP_005468.1:n.1590+48dup
Search 100 bp 5'
Search 100 bp 3'