Canonical Allele Identifier: CA2736012699
Gene: IL11 HGNC NCBI

Linked Data

dbSNP Id: rs2123242266
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55368406A>G , CM000681.2:g.55368406A>G GRCh38
NC_000019.9:g.55879774A>G , CM000681.1:g.55879774A>G GRCh37
NC_000019.8:g.60571586A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264563.7:c.268-35T>C MANE Select ENSP00000264563.1:n.268-35T>C
ENST00000264563.6:c.268-35T>C ENSP00000264563.1:n.268-35T>C
ENST00000585513.1:c.268-35T>C ENSP00000467355.1:n.268-35T>C
ENST00000587093.1:c.31-35T>C ENSP00000468663.1:n.31-35T>C
ENST00000590625.5:c.31-35T>C ENSP00000465705.1:n.31-35T>C
NM_000641.3:c.268-35T>C NP_000632.1:n.268-35T>C
NM_001267718.1:c.31-35T>C NP_001254647.1:n.31-35T>C
NM_000641.4:c.268-35T>C MANE Select NP_000632.1:n.268-35T>C
NM_001267718.2:c.31-35T>C NP_001254647.1:n.31-35T>C
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