Canonical Allele Identifier: CA535229461
Gene: IL1F10 HGNC NCBI

Linked Data

dbSNP Id: rs1484682065
gnomAD v2: 2-113832319-TA-T
gnomAD v3: 2-113074742-TA-T
gnomAD v4: 2-113074742-TA-T
MyVariant Identifiers: chr2:g.113832320del (hg19) chr2:g.113074743del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074744del , CM000664.2:g.113074744del GRCh38
NC_000002.11:g.113832321del , CM000664.1:g.113832321del GRCh37
NC_000002.10:g.113548792del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.140del ENSP00000376893.2:p.Asn47ThrfsTer?
ENST00000341010.6:c.140del MANE Select ENSP00000341794.2:p.Asn47ThrfsTer?
ENST00000393197.2:c.140del ENSP00000376893.2:p.Asn47ThrfsTer?
ENST00000496265.1:n.206del
NM_032556.5:c.140del NP_115945.4:p.Asn47ThrfsTer?
NM_173161.2:c.140del NP_775184.1:p.Asn47ThrfsTer?
NM_032556.6:c.140del NP_115945.4:p.Asn47ThrfsTer?
NM_173161.3:c.140del MANE Select NP_775184.1:p.Asn47ThrfsTer?
Search 100 bp 5'
Search 100 bp 3'