Canonical Allele Identifier: CA36551341

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs957750213
• MyVariant Identifiers: chr1:g.206946288A>G (hg19) ; chr1:g.206772943A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772943A>G , CM000663.2:g.206772943A>G	GRCh38
NC_000001.10:g.206946288A>G , CM000663.1:g.206946288A>G	GRCh37
NC_000001.9:g.205012911A>G	NCBI36
NG_012088.1:g.4552T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-14-611T>C (IL10)	ENSP00000499588.1:n.-14-611T>C
ENST00000659642.2:c.-625T>C (IL10)	ENSP00000499509.1:n.-625T>C
ENST00000664374.2:c.-14-611T>C (IL10)	ENSP00000499664.1:n.-14-611T>C
ENST00000659997.3:c.-149+1865A>G (IL19) MANE Select	ENSP00000499459.2:n.-149+1865A>G
ENST00000656872.2:c.-149+2113A>G (IL19)	ENSP00000499487.2:n.-149+2113A>G
ENST00000659065.1:c.-14-611T>C (IL10)	ENSP00000499588.1:n.-14-611T>C
ENST00000659642.1:c.-625T>C (IL10)	ENSP00000499509.1:n.-625T>C
ENST00000659997.2:c.-149+1865A>G (IL19)	ENSP00000499459.2:n.-149+1865A>G
ENST00000662320.1:n.67+2113A>G (IL19)
ENST00000664374.1:c.-14-611T>C (IL10)	ENSP00000499664.1:n.-14-611T>C
XM_011509506.1:c.-508T>C (IL10)	XP_011507808.1:n.-508T>C
NM_153758.3:c.-35+1865A>G (IL19)	NP_715639.1:n.-35+1865A>G
NM_001393490.1:c.-149+2113A>G (IL19)	NP_001380419.1:n.-149+2113A>G
NM_153758.5:c.-149+1865A>G (IL19) MANE Select	NP_715639.2:n.-149+1865A>G