Canonical Allele Identifier: CA407457424

Gene: IL11

Linked Data

• MyVariant Identifiers: chr19:g.55879879A>C (hg19) ; chr19:g.55368511A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55368511A>C , CM000681.2:g.55368511A>C	GRCh38
NC_000019.9:g.55879879A>C , CM000681.1:g.55879879A>C	GRCh37
NC_000019.8:g.60571691A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.239T>G MANE Select	ENSP00000264563.1:p.Met80Arg
ENST00000264563.6:c.239T>G	ENSP00000264563.1:p.Met80Arg
ENST00000585513.1:c.239T>G	ENSP00000467355.1:p.Met80Arg
ENST00000587093.1:c.2T>G	ENSP00000468663.1:p.Met1Arg
ENST00000590625.5:c.2T>G	ENSP00000465705.1:p.Met1Arg
NM_000641.3:c.239T>G	NP_000632.1:p.Met80Arg
NM_001267718.1:c.2T>G	NP_001254647.1:p.Met1Arg
NM_000641.4:c.239T>G MANE Select	NP_000632.1:p.Met80Arg
NM_001267718.2:c.2T>G	NP_001254647.1:p.Met1Arg