Canonical Allele Identifier: CA2577074739
Gene: IL1F10 HGNC NCBI

Linked Data

gnomAD v4: 2-113074645-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074645T>C , CM000664.2:g.113074645T>C GRCh38
NC_000002.11:g.113832222T>C , CM000664.1:g.113832222T>C GRCh37
NC_000002.10:g.113548693T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.119-78T>C ENSP00000376893.2:n.119-78T>C
ENST00000341010.6:c.119-78T>C MANE Select ENSP00000341794.2:n.119-78T>C
ENST00000393197.2:c.119-78T>C ENSP00000376893.2:n.119-78T>C
ENST00000496265.1:n.107T>C
NM_032556.5:c.119-78T>C NP_115945.4:n.119-78T>C
NM_173161.2:c.119-78T>C NP_775184.1:n.119-78T>C
NM_032556.6:c.119-78T>C NP_115945.4:n.119-78T>C
NM_173161.3:c.119-78T>C MANE Select NP_775184.1:n.119-78T>C
Search 100 bp 5'
Search 100 bp 3'