Canonical Allele Identifier: CA2736012719
Gene: IL11 HGNC NCBI

Linked Data

dbSNP Id: rs2123242289
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55368426C>T , CM000681.2:g.55368426C>T GRCh38
NC_000019.9:g.55879794C>T , CM000681.1:g.55879794C>T GRCh37
NC_000019.8:g.60571606C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264563.7:c.268-55G>A MANE Select ENSP00000264563.1:n.268-55G>A
ENST00000264563.6:c.268-55G>A ENSP00000264563.1:n.268-55G>A
ENST00000585513.1:c.268-55G>A ENSP00000467355.1:n.268-55G>A
ENST00000587093.1:c.31-55G>A ENSP00000468663.1:n.31-55G>A
ENST00000590625.5:c.31-55G>A ENSP00000465705.1:n.31-55G>A
NM_000641.3:c.268-55G>A NP_000632.1:n.268-55G>A
NM_001267718.1:c.31-55G>A NP_001254647.1:n.31-55G>A
NM_000641.4:c.268-55G>A MANE Select NP_000632.1:n.268-55G>A
NM_001267718.2:c.31-55G>A NP_001254647.1:n.31-55G>A
Search 100 bp 5'
Search 100 bp 3'