Canonical Allele Identifier: CA348292185
Gene: IL1F10 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.142A>G ENSP00000376893.2:p.Arg48Gly
ENST00000341010.6:c.142A>G MANE Select ENSP00000341794.2:p.Arg48Gly
ENST00000393197.2:c.142A>G ENSP00000376893.2:p.Arg48Gly
ENST00000496265.1:n.208A>G
NM_032556.5:c.142A>G NP_115945.4:p.Arg48Gly
NM_173161.2:c.142A>G NP_775184.1:p.Arg48Gly
NM_032556.6:c.142A>G NP_115945.4:p.Arg48Gly
NM_173161.3:c.142A>G MANE Select NP_775184.1:p.Arg48Gly