Canonical Allele Identifier: CA1280046133
Gene: IL1F10 HGNC NCBI

Linked Data

dbSNP Id: rs1685902821

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074648C>T , CM000664.2:g.113074648C>T GRCh38
NC_000002.11:g.113832225C>T , CM000664.1:g.113832225C>T GRCh37
NC_000002.10:g.113548696C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.119-75C>T ENSP00000376893.2:n.119-75C>T
ENST00000341010.6:c.119-75C>T MANE Select ENSP00000341794.2:n.119-75C>T
ENST00000393197.2:c.119-75C>T ENSP00000376893.2:n.119-75C>T
ENST00000496265.1:n.110C>T
NM_032556.5:c.119-75C>T NP_115945.4:n.119-75C>T
NM_173161.2:c.119-75C>T NP_775184.1:n.119-75C>T
NM_032556.6:c.119-75C>T NP_115945.4:n.119-75C>T
NM_173161.3:c.119-75C>T MANE Select NP_775184.1:n.119-75C>T