Canonical Allele Identifier: CA344481971

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944278T>A (hg19) ; chr1:g.206770933T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770933T>A , CM000663.2:g.206770933T>A	GRCh38
NC_000001.10:g.206944278T>A , CM000663.1:g.206944278T>A	GRCh37
NC_000001.9:g.205010901T>A	NCBI36
NG_012088.1:g.6562A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.257A>T (IL10)
ENST00000471071.2:c.97A>T (IL10)	ENSP00000493073.2:p.Thr33Ser
ENST00000659065.2:c.235A>T (IL10)	ENSP00000499588.1:p.Thr79Ser
ENST00000659642.2:c.235A>T (IL10)	ENSP00000499509.1:p.Thr79Ser
ENST00000664374.2:c.235A>T (IL10)	ENSP00000499664.1:p.Thr79Ser
ENST00000659997.3:c.-294T>A (IL19) MANE Select	ENSP00000499459.2:n.-294T>A
ENST00000656872.2:c.-149+103T>A (IL19)	ENSP00000499487.2:n.-149+103T>A
ENST00000659065.1:c.235A>T (IL10)	ENSP00000499588.1:p.Thr79Ser
ENST00000659642.1:c.235A>T (IL10)	ENSP00000499509.1:p.Thr79Ser
ENST00000659997.2:c.-294T>A (IL19)	ENSP00000499459.2:n.-294T>A
ENST00000662320.1:n.67+103T>A (IL19)
ENST00000664374.1:c.235A>T (IL10)	ENSP00000499664.1:p.Thr79Ser
ENST00000367099.3:n.257A>T (IL10)
ENST00000423557.1:c.352A>T (IL10) MANE Select	ENSP00000412237.1:p.Thr118Ser
ENST00000471071.1:n.267A>T (IL10)
NM_000572.2:c.352A>T (IL10)	NP_000563.1:p.Thr118Ser
XM_011509506.1:c.352A>T (IL10)	XP_011507808.1:p.Thr118Ser
NM_000572.3:c.352A>T (IL10) MANE Select	NP_000563.1:p.Thr118Ser
NM_153758.3:c.-180T>A (IL19)	NP_715639.1:n.-180T>A
NM_001382624.1:c.97A>T (IL10)	NP_001369553.1:p.Thr33Ser
NM_001393490.1:c.-149+103T>A (IL19)	NP_001380419.1:n.-149+103T>A
NM_153758.5:c.-294T>A (IL19) MANE Select	NP_715639.2:n.-294T>A
NR_168466.1:n.411A>T (IL10)