Canonical Allele Identifier: CA344482102

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs2102439246
• MyVariant Identifiers: chr1:g.206944338C>T (hg19) ; chr1:g.206770993C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770993C>T , CM000663.2:g.206770993C>T	GRCh38
NC_000001.10:g.206944338C>T , CM000663.1:g.206944338C>T	GRCh37
NC_000001.9:g.205010961C>T	NCBI36
NG_012088.1:g.6502G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.197G>A (IL10)
ENST00000471071.2:c.37G>A (IL10)	ENSP00000493073.2:p.Ala13Thr
ENST00000659065.2:c.175G>A (IL10)	ENSP00000499588.1:p.Ala59Thr
ENST00000659642.2:c.175G>A (IL10)	ENSP00000499509.1:p.Ala59Thr
ENST00000664374.2:c.175G>A (IL10)	ENSP00000499664.1:p.Ala59Thr
ENST00000659997.3:c.-234C>T (IL19) MANE Select	ENSP00000499459.2:n.-234C>T
ENST00000656872.2:c.-149+163C>T (IL19)	ENSP00000499487.2:n.-149+163C>T
ENST00000659065.1:c.175G>A (IL10)	ENSP00000499588.1:p.Ala59Thr
ENST00000659642.1:c.175G>A (IL10)	ENSP00000499509.1:p.Ala59Thr
ENST00000659997.2:c.-234C>T (IL19)	ENSP00000499459.2:n.-234C>T
ENST00000662320.1:n.67+163C>T (IL19)
ENST00000664374.1:c.175G>A (IL10)	ENSP00000499664.1:p.Ala59Thr
ENST00000367099.3:n.197G>A (IL10)
ENST00000423557.1:c.292G>A (IL10) MANE Select	ENSP00000412237.1:p.Ala98Thr
ENST00000471071.1:n.207G>A (IL10)
NM_000572.2:c.292G>A (IL10)	NP_000563.1:p.Ala98Thr
XM_011509506.1:c.292G>A (IL10)	XP_011507808.1:p.Ala98Thr
NM_000572.3:c.292G>A (IL10) MANE Select	NP_000563.1:p.Ala98Thr
NM_153758.3:c.-120C>T (IL19)	NP_715639.1:n.-120C>T
NM_001382624.1:c.37G>A (IL10)	NP_001369553.1:p.Ala13Thr
NM_001393490.1:c.-149+163C>T (IL19)	NP_001380419.1:n.-149+163C>T
NM_153758.5:c.-234C>T (IL19) MANE Select	NP_715639.2:n.-234C>T
NR_168466.1:n.351G>A (IL10)