Canonical Allele Identifier: CA1280046200
Gene: IL1F10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074747G= , CM000664.2:g.113074747G= GRCh38
NC_000002.11:g.113832324G= , CM000664.1:g.113832324G= GRCh37
NC_000002.10:g.113548795G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.143G= ENSP00000376893.2:p.Arg48=
ENST00000341010.6:c.143G= MANE Select ENSP00000341794.2:p.Arg48=
ENST00000393197.2:c.143G= ENSP00000376893.2:p.Arg48=
ENST00000496265.1:n.209G=
NM_032556.5:c.143G= NP_115945.4:p.Arg48=
NM_173161.2:c.143G= NP_775184.1:p.Arg48=
NM_032556.6:c.143G= NP_115945.4:p.Arg48=
NM_173161.3:c.143G= MANE Select NP_775184.1:p.Arg48=