Canonical Allele Identifier: CA2587294973
Gene: IL11 HGNC NCBI

Linked Data

gnomAD v4: 19-55368417-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55368417T>C , CM000681.2:g.55368417T>C GRCh38
NC_000019.9:g.55879785T>C , CM000681.1:g.55879785T>C GRCh37
NC_000019.8:g.60571597T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264563.7:c.268-46A>G MANE Select ENSP00000264563.1:n.268-46A>G
ENST00000264563.6:c.268-46A>G ENSP00000264563.1:n.268-46A>G
ENST00000585513.1:c.268-46A>G ENSP00000467355.1:n.268-46A>G
ENST00000587093.1:c.31-46A>G ENSP00000468663.1:n.31-46A>G
ENST00000590625.5:c.31-46A>G ENSP00000465705.1:n.31-46A>G
NM_000641.3:c.268-46A>G NP_000632.1:n.268-46A>G
NM_001267718.1:c.31-46A>G NP_001254647.1:n.31-46A>G
NM_000641.4:c.268-46A>G MANE Select NP_000632.1:n.268-46A>G
NM_001267718.2:c.31-46A>G NP_001254647.1:n.31-46A>G
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