Canonical Allele Identifier: CA348292182
Gene: IL1F10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113832321A>T (hg19) chr2:g.113074744A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.140A>T ENSP00000376893.2:p.Asn47Ile
ENST00000341010.6:c.140A>T MANE Select ENSP00000341794.2:p.Asn47Ile
ENST00000393197.2:c.140A>T ENSP00000376893.2:p.Asn47Ile
ENST00000496265.1:n.206A>T
NM_032556.5:c.140A>T NP_115945.4:p.Asn47Ile
NM_173161.2:c.140A>T NP_775184.1:p.Asn47Ile
NM_032556.6:c.140A>T NP_115945.4:p.Asn47Ile
NM_173161.3:c.140A>T MANE Select NP_775184.1:p.Asn47Ile
Search 100 bp 5'
Search 100 bp 3'