Canonical Allele Identifier: CA2697948593

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs2102441821

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773149T>A , CM000663.2:g.206773149T>A	GRCh38
NC_000001.10:g.206946494T>A , CM000663.1:g.206946494T>A	GRCh37
NC_000001.9:g.205013117T>A	NCBI36
NG_012088.1:g.4346A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+531A>T (IL10)	ENSP00000499588.1:n.-15+531A>T
ENST00000659642.2:c.-831A>T (IL10)	ENSP00000499509.1:n.-831A>T
ENST00000664374.2:c.-14-817A>T (IL10)	ENSP00000499664.1:n.-14-817A>T
ENST00000659997.3:c.-149+2071T>A (IL19) MANE Select	ENSP00000499459.2:n.-149+2071T>A
ENST00000656872.2:c.-149+2319T>A (IL19)	ENSP00000499487.2:n.-149+2319T>A
ENST00000659065.1:c.-15+531A>T (IL10)	ENSP00000499588.1:n.-15+531A>T
ENST00000659642.1:c.-831A>T (IL10)	ENSP00000499509.1:n.-831A>T
ENST00000659997.2:c.-149+2071T>A (IL19)	ENSP00000499459.2:n.-149+2071T>A
ENST00000662320.1:n.67+2319T>A (IL19)
ENST00000664374.1:c.-14-817A>T (IL10)	ENSP00000499664.1:n.-14-817A>T
XM_011509506.1:c.-714A>T (IL10)	XP_011507808.1:n.-714A>T
NM_153758.3:c.-35+2071T>A (IL19)	NP_715639.1:n.-35+2071T>A
NM_001393490.1:c.-149+2319T>A (IL19)	NP_001380419.1:n.-149+2319T>A
NM_153758.5:c.-149+2071T>A (IL19) MANE Select	NP_715639.2:n.-149+2071T>A