Canonical Allele Identifier: CA348292177
Gene: IL1F10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113832320A>C (hg19) chr2:g.113074743A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074743A>C , CM000664.2:g.113074743A>C GRCh38
NC_000002.11:g.113832320A>C , CM000664.1:g.113832320A>C GRCh37
NC_000002.10:g.113548791A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.139A>C ENSP00000376893.2:p.Asn47His
ENST00000341010.6:c.139A>C MANE Select ENSP00000341794.2:p.Asn47His
ENST00000393197.2:c.139A>C ENSP00000376893.2:p.Asn47His
ENST00000496265.1:n.205A>C
NM_032556.5:c.139A>C NP_115945.4:p.Asn47His
NM_173161.2:c.139A>C NP_775184.1:p.Asn47His
NM_032556.6:c.139A>C NP_115945.4:p.Asn47His
NM_173161.3:c.139A>C MANE Select NP_775184.1:p.Asn47His
Search 100 bp 5'
Search 100 bp 3'