Canonical Allele Identifier: CA348292188

Gene: IL1F10

Linked Data

• MyVariant Identifiers: chr2:g.113832324G>T (hg19) ; chr2:g.113074747G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393197.3:c.143G>T	ENSP00000376893.2:p.Arg48Ile
ENST00000341010.6:c.143G>T MANE Select	ENSP00000341794.2:p.Arg48Ile
ENST00000393197.2:c.143G>T	ENSP00000376893.2:p.Arg48Ile
ENST00000496265.1:n.209G>T
NM_032556.5:c.143G>T	NP_115945.4:p.Arg48Ile
NM_173161.2:c.143G>T	NP_775184.1:p.Arg48Ile
NM_032556.6:c.143G>T	NP_115945.4:p.Arg48Ile
NM_173161.3:c.143G>T MANE Select	NP_775184.1:p.Arg48Ile