Canonical Allele Identifier: CA36551962

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs139002227
• MyVariant Identifiers: chr1:g.206947072G>T (hg19) ; chr1:g.206773727G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773727G>T , CM000663.2:g.206773727G>T	GRCh38
NC_000001.10:g.206947072G>T , CM000663.1:g.206947072G>T	GRCh37
NC_000001.9:g.205013695G>T	NCBI36
NG_012088.1:g.3768C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-62C>A (IL10)	ENSP00000499588.1:n.-62C>A
ENST00000659642.2:c.-1118-291C>A (IL10)	ENSP00000499509.1:n.-1118-291C>A
ENST00000664374.2:c.-15+603C>A (IL10)	ENSP00000499664.1:n.-15+603C>A
ENST00000659997.3:c.-149+2649G>T (IL19) MANE Select	ENSP00000499459.2:n.-149+2649G>T
ENST00000656872.2:c.-149+2897G>T (IL19)	ENSP00000499487.2:n.-149+2897G>T
ENST00000659065.1:c.-62C>A (IL10)	ENSP00000499588.1:n.-62C>A
ENST00000659642.1:c.-1118-291C>A (IL10)	ENSP00000499509.1:n.-1118-291C>A
ENST00000659997.2:c.-149+2649G>T (IL19)	ENSP00000499459.2:n.-149+2649G>T
ENST00000662320.1:n.67+2897G>T (IL19)
ENST00000664374.1:c.-15+603C>A (IL10)	ENSP00000499664.1:n.-15+603C>A
XM_011509506.1:c.-1001-291C>A (IL10)	XP_011507808.1:n.-1001-291C>A
NM_153758.3:c.-35+2649G>T (IL19)	NP_715639.1:n.-35+2649G>T
NM_001393490.1:c.-149+2897G>T (IL19)	NP_001380419.1:n.-149+2897G>T
NM_153758.5:c.-149+2649G>T (IL19) MANE Select	NP_715639.2:n.-149+2649G>T