Canonical Allele Identifier: CA272672357
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs752802155
MyVariant Identifiers: chr15:g.73622390del (hg19) chr15:g.73330049del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330050del , CM000677.2:g.73330050del GRCh38
NC_000015.9:g.73622391del , CM000677.1:g.73622391del GRCh37
NC_000015.8:g.71409444del NCBI36
NG_009063.1:g.44216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-258del MANE Select ENSP00000261917.3:n.1372-258del
ENST00000261917.3:c.1372-258del ENSP00000261917.3:n.1372-258del
NM_005477.2:c.1372-258del NP_005468.1:n.1372-258del
XM_011521148.1:c.154-258del XP_011519450.1:n.154-258del
XM_011521148.2:c.154-258del XP_011519450.1:n.154-258del
NM_005477.3:c.1372-258del MANE Select NP_005468.1:n.1372-258del
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