Canonical Allele Identifier: CA2587294982
Gene: IL11 HGNC NCBI

Linked Data

gnomAD v4: 19-55368429-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55368429C>T , CM000681.2:g.55368429C>T GRCh38
NC_000019.9:g.55879797C>T , CM000681.1:g.55879797C>T GRCh37
NC_000019.8:g.60571609C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264563.7:c.267+54G>A MANE Select ENSP00000264563.1:n.267+54G>A
ENST00000264563.6:c.267+54G>A ENSP00000264563.1:n.267+54G>A
ENST00000585513.1:c.267+54G>A ENSP00000467355.1:n.267+54G>A
ENST00000587093.1:c.30+54G>A ENSP00000468663.1:n.30+54G>A
ENST00000590625.5:c.30+54G>A ENSP00000465705.1:n.30+54G>A
NM_000641.3:c.267+54G>A NP_000632.1:n.267+54G>A
NM_001267718.1:c.30+54G>A NP_001254647.1:n.30+54G>A
NM_000641.4:c.267+54G>A MANE Select NP_000632.1:n.267+54G>A
NM_001267718.2:c.30+54G>A NP_001254647.1:n.30+54G>A
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