Canonical Allele Identifier: CA407457408

Gene: IL11

Linked Data

• MyVariant Identifiers: chr19:g.55879877T>C (hg19) ; chr19:g.55368509T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55368509T>C , CM000681.2:g.55368509T>C	GRCh38
NC_000019.9:g.55879877T>C , CM000681.1:g.55879877T>C	GRCh37
NC_000019.8:g.60571689T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.241A>G MANE Select	ENSP00000264563.1:p.Ser81Gly
ENST00000264563.6:c.241A>G	ENSP00000264563.1:p.Ser81Gly
ENST00000585513.1:c.241A>G	ENSP00000467355.1:p.Ser81Gly
ENST00000587093.1:c.4A>G	ENSP00000468663.1:p.Ser2Gly
ENST00000590625.5:c.4A>G	ENSP00000465705.1:p.Ser2Gly
NM_000641.3:c.241A>G	NP_000632.1:p.Ser81Gly
NM_001267718.1:c.4A>G	NP_001254647.1:p.Ser2Gly
NM_000641.4:c.241A>G MANE Select	NP_000632.1:p.Ser81Gly
NM_001267718.2:c.4A>G	NP_001254647.1:p.Ser2Gly