Canonical Allele Identifier: CA36551392

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs949216200
• MyVariant Identifiers: chr1:g.206946356A>C (hg19) ; chr1:g.206773011A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773011A>C , CM000663.2:g.206773011A>C	GRCh38
NC_000001.10:g.206946356A>C , CM000663.1:g.206946356A>C	GRCh37
NC_000001.9:g.205012979A>C	NCBI36
NG_012088.1:g.4484T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+669T>G (IL10)	ENSP00000499588.1:n.-15+669T>G
ENST00000659642.2:c.-693T>G (IL10)	ENSP00000499509.1:n.-693T>G
ENST00000664374.2:c.-14-679T>G (IL10)	ENSP00000499664.1:n.-14-679T>G
ENST00000659997.3:c.-149+1933A>C (IL19) MANE Select	ENSP00000499459.2:n.-149+1933A>C
ENST00000656872.2:c.-149+2181A>C (IL19)	ENSP00000499487.2:n.-149+2181A>C
ENST00000659065.1:c.-15+669T>G (IL10)	ENSP00000499588.1:n.-15+669T>G
ENST00000659642.1:c.-693T>G (IL10)	ENSP00000499509.1:n.-693T>G
ENST00000659997.2:c.-149+1933A>C (IL19)	ENSP00000499459.2:n.-149+1933A>C
ENST00000662320.1:n.67+2181A>C (IL19)
ENST00000664374.1:c.-14-679T>G (IL10)	ENSP00000499664.1:n.-14-679T>G
XM_011509506.1:c.-576T>G (IL10)	XP_011507808.1:n.-576T>G
NM_153758.3:c.-35+1933A>C (IL19)	NP_715639.1:n.-35+1933A>C
NM_001393490.1:c.-149+2181A>C (IL19)	NP_001380419.1:n.-149+2181A>C
NM_153758.5:c.-149+1933A>C (IL19) MANE Select	NP_715639.2:n.-149+1933A>C