Canonical Allele Identifier: CA1140144101
Gene: ILF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153668351C= , CM000663.2:g.153668351C= GRCh38
NC_000001.10:g.153640827C= , CM000663.1:g.153640827C= GRCh37
NC_000001.9:g.151907451C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361891.9:c.213+102G= MANE Select ENSP00000355011.4:n.213+102G=
ENST00000361891.8:c.213+102G= ENSP00000355011.4:n.213+102G=
ENST00000368681.1:c.213+102G= ENSP00000357670.1:n.213+102G=
ENST00000368684.8:c.99+102G= ENSP00000357673.4:n.99+102G=
ENST00000615950.4:c.99+102G= ENSP00000482909.1:n.99+102G=
NM_001267809.1:c.99+102G= NP_001254738.1:n.99+102G=
NM_004515.3:c.213+102G= NP_004506.2:n.213+102G=
NM_004515.4:c.213+102G= MANE Select NP_004506.2:n.213+102G=
NM_001267809.2:c.99+102G= NP_001254738.1:n.99+102G=