Canonical Allele Identifier: CA407457400

Gene: IL11

Linked Data

• gnomAD v4: 19-55368508-C-T
• MyVariant Identifiers: chr19:g.55879876C>T (hg19) ; chr19:g.55368508C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55368508C>T , CM000681.2:g.55368508C>T	GRCh38
NC_000019.9:g.55879876C>T , CM000681.1:g.55879876C>T	GRCh37
NC_000019.8:g.60571688C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.242G>A MANE Select	ENSP00000264563.1:p.Ser81Asn
ENST00000264563.6:c.242G>A	ENSP00000264563.1:p.Ser81Asn
ENST00000585513.1:c.242G>A	ENSP00000467355.1:p.Ser81Asn
ENST00000587093.1:c.5G>A	ENSP00000468663.1:p.Ser2Asn
ENST00000590625.5:c.5G>A	ENSP00000465705.1:p.Ser2Asn
NM_000641.3:c.242G>A	NP_000632.1:p.Ser81Asn
NM_001267718.1:c.5G>A	NP_001254647.1:p.Ser2Asn
NM_000641.4:c.242G>A MANE Select	NP_000632.1:p.Ser81Asn
NM_001267718.2:c.5G>A	NP_001254647.1:p.Ser2Asn