Canonical Allele Identifier: CA428301649

Gene: IL1F10

Linked Data

• MyVariant Identifiers: chr2:g.113832313A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113074736A>T , CM000664.2:g.113074736A>T	GRCh38
NC_000002.11:g.113832313A>T , CM000664.1:g.113832313A>T	GRCh37
NC_000002.10:g.113548784A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393197.3:c.132A>T	ENSP00000376893.2:p.Ile44=
ENST00000341010.6:c.132A>T MANE Select	ENSP00000341794.2:p.Ile44=
ENST00000393197.2:c.132A>T	ENSP00000376893.2:p.Ile44=
ENST00000496265.1:n.198A>T
NM_032556.5:c.132A>T	NP_115945.4:p.Ile44=
NM_173161.2:c.132A>T	NP_775184.1:p.Ile44=
NM_032556.6:c.132A>T	NP_115945.4:p.Ile44=
NM_173161.3:c.132A>T MANE Select	NP_775184.1:p.Ile44=