Canonical Allele Identifier: CA348292189
Gene: IL1F10 HGNC NCBI

Linked Data

dbSNP Id: rs1288553577
gnomAD v3: 2-113074747-G-C
gnomAD v4: 2-113074747-G-C
MyVariant Identifiers: chr2:g.113832324G>C (hg19) chr2:g.113074747G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.143G>C ENSP00000376893.2:p.Arg48Thr
ENST00000341010.6:c.143G>C MANE Select ENSP00000341794.2:p.Arg48Thr
ENST00000393197.2:c.143G>C ENSP00000376893.2:p.Arg48Thr
ENST00000496265.1:n.209G>C
NM_032556.5:c.143G>C NP_115945.4:p.Arg48Thr
NM_173161.2:c.143G>C NP_775184.1:p.Arg48Thr
NM_032556.6:c.143G>C NP_115945.4:p.Arg48Thr
NM_173161.3:c.143G>C MANE Select NP_775184.1:p.Arg48Thr
Search 100 bp 5'
Search 100 bp 3'