Canonical Allele Identifier: CA528575012

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1352649317
• gnomAD v2: 1-206947118-A-G
• gnomAD v3: 1-206773773-A-G
• gnomAD v4: 1-206773773-A-G
• MyVariant Identifiers: chr1:g.206947118A>G (hg19) ; chr1:g.206773773A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773773A>G , CM000663.2:g.206773773A>G	GRCh38
NC_000001.10:g.206947118A>G , CM000663.1:g.206947118A>G	GRCh37
NC_000001.9:g.205013741A>G	NCBI36
NG_012088.1:g.3722T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-108T>C (IL10)	ENSP00000499588.1:n.-108T>C
ENST00000659642.2:c.-1118-337T>C (IL10)	ENSP00000499509.1:n.-1118-337T>C
ENST00000664374.2:c.-15+557T>C (IL10)	ENSP00000499664.1:n.-15+557T>C
ENST00000659997.3:c.-149+2695A>G (IL19) MANE Select	ENSP00000499459.2:n.-149+2695A>G
ENST00000656872.2:c.-149+2943A>G (IL19)	ENSP00000499487.2:n.-149+2943A>G
ENST00000659065.1:c.-108T>C (IL10)	ENSP00000499588.1:n.-108T>C
ENST00000659642.1:c.-1118-337T>C (IL10)	ENSP00000499509.1:n.-1118-337T>C
ENST00000659997.2:c.-149+2695A>G (IL19)	ENSP00000499459.2:n.-149+2695A>G
ENST00000662320.1:n.67+2943A>G (IL19)
ENST00000664374.1:c.-15+557T>C (IL10)	ENSP00000499664.1:n.-15+557T>C
XM_011509506.1:c.-1001-337T>C (IL10)	XP_011507808.1:n.-1001-337T>C
NM_153758.3:c.-35+2695A>G (IL19)	NP_715639.1:n.-35+2695A>G
NM_001393490.1:c.-149+2943A>G (IL19)	NP_001380419.1:n.-149+2943A>G
NM_153758.5:c.-149+2695A>G (IL19) MANE Select	NP_715639.2:n.-149+2695A>G