Canonical Allele Identifier: CA1280046129
Gene: IL1F10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074644C= , CM000664.2:g.113074644C= GRCh38
NC_000002.11:g.113832221C= , CM000664.1:g.113832221C= GRCh37
NC_000002.10:g.113548692C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.119-79C= ENSP00000376893.2:n.119-79C=
ENST00000341010.6:c.119-79C= MANE Select ENSP00000341794.2:n.119-79C=
ENST00000393197.2:c.119-79C= ENSP00000376893.2:n.119-79C=
ENST00000496265.1:n.106C=
NM_032556.5:c.119-79C= NP_115945.4:n.119-79C=
NM_173161.2:c.119-79C= NP_775184.1:n.119-79C=
NM_032556.6:c.119-79C= NP_115945.4:n.119-79C=
NM_173161.3:c.119-79C= MANE Select NP_775184.1:n.119-79C=