Canonical Allele Identifier: CA428301665
Gene: IL1F10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113832323A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074746A>C , CM000664.2:g.113074746A>C GRCh38
NC_000002.11:g.113832323A>C , CM000664.1:g.113832323A>C GRCh37
NC_000002.10:g.113548794A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.142A>C ENSP00000376893.2:p.Arg48=
ENST00000341010.6:c.142A>C MANE Select ENSP00000341794.2:p.Arg48=
ENST00000393197.2:c.142A>C ENSP00000376893.2:p.Arg48=
ENST00000496265.1:n.208A>C
NM_032556.5:c.142A>C NP_115945.4:p.Arg48=
NM_173161.2:c.142A>C NP_775184.1:p.Arg48=
NM_032556.6:c.142A>C NP_115945.4:p.Arg48=
NM_173161.3:c.142A>C MANE Select NP_775184.1:p.Arg48=
Search 100 bp 5'
Search 100 bp 3'