Canonical Allele Identifier: CA393098979
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1262682298
MyVariant Identifiers: chr15:g.73660493_73660494insG (hg19) chr15:g.73368152_73368153insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368154dup , CM000677.2:g.73368154dup GRCh38
NC_000015.9:g.73660495dup , CM000677.1:g.73660495dup GRCh37
NC_000015.8:g.71447548dup NCBI36
NG_009063.1:g.6112dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.118dup MANE Select ENSP00000261917.3:p.Arg40ProfsTer?
ENST00000261917.3:c.118dup ENSP00000261917.3:p.Arg40ProfsTer?
NM_005477.2:c.118dup NP_005468.1:p.Arg40ProfsTer?
NM_005477.3:c.118dup MANE Select NP_005468.1:p.Arg40ProfsTer?
Search 100 bp 5'
Search 100 bp 3'