Canonical Allele Identifier: CA1838563
Gene: IL1F10 HGNC NCBI

Linked Data

dbSNP Id: rs533273391
ExAC: 2:113832223 G / T
gnomAD v2: 2-113832223-G-T
gnomAD v3: 2-113074646-G-T
gnomAD v4: 2-113074646-G-T
MyVariant Identifiers: chr2:g.113832223G>T (hg19) chr2:g.113074646G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113074646G>T , CM000664.2:g.113074646G>T GRCh38
NC_000002.11:g.113832223G>T , CM000664.1:g.113832223G>T GRCh37
NC_000002.10:g.113548694G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393197.3:c.119-77G>T ENSP00000376893.2:n.119-77G>T
ENST00000341010.6:c.119-77G>T MANE Select ENSP00000341794.2:n.119-77G>T
ENST00000393197.2:c.119-77G>T ENSP00000376893.2:n.119-77G>T
ENST00000496265.1:n.108G>T
NM_032556.5:c.119-77G>T NP_115945.4:n.119-77G>T
NM_173161.2:c.119-77G>T NP_775184.1:n.119-77G>T
NM_032556.6:c.119-77G>T NP_115945.4:n.119-77G>T
NM_173161.3:c.119-77G>T MANE Select NP_775184.1:n.119-77G>T
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