Canonical Allele Identifier: CA9674249

Gene: IL11

Linked Data

• dbSNP Id: rs779248310
• ExAC: 19:55879874 C / T
• gnomAD v4: 19-55368506-C-T
• MyVariant Identifiers: chr19:g.55879874C>T (hg19) ; chr19:g.55368506C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55368506C>T , CM000681.2:g.55368506C>T	GRCh38
NC_000019.9:g.55879874C>T , CM000681.1:g.55879874C>T	GRCh37
NC_000019.8:g.60571686C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.244G>A MANE Select	ENSP00000264563.1:p.Ala82Thr
ENST00000264563.6:c.244G>A	ENSP00000264563.1:p.Ala82Thr
ENST00000585513.1:c.244G>A	ENSP00000467355.1:p.Ala82Thr
ENST00000587093.1:c.7G>A	ENSP00000468663.1:p.Ala3Thr
ENST00000590625.5:c.7G>A	ENSP00000465705.1:p.Ala3Thr
NM_000641.3:c.244G>A	NP_000632.1:p.Ala82Thr
NM_001267718.1:c.7G>A	NP_001254647.1:p.Ala3Thr
NM_000641.4:c.244G>A MANE Select	NP_000632.1:p.Ala82Thr
NM_001267718.2:c.7G>A	NP_001254647.1:p.Ala3Thr