Canonical Allele Identifier: CA36551557

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1032417882
• gnomAD v3: 1-206773167-C-T
• gnomAD v4: 1-206773167-C-T
• MyVariant Identifiers: chr1:g.206946512C>T (hg19) ; chr1:g.206773167C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773167C>T , CM000663.2:g.206773167C>T	GRCh38
NC_000001.10:g.206946512C>T , CM000663.1:g.206946512C>T	GRCh37
NC_000001.9:g.205013135C>T	NCBI36
NG_012088.1:g.4328G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+513G>A (IL10)	ENSP00000499588.1:n.-15+513G>A
ENST00000659642.2:c.-849G>A (IL10)	ENSP00000499509.1:n.-849G>A
ENST00000664374.2:c.-14-835G>A (IL10)	ENSP00000499664.1:n.-14-835G>A
ENST00000659997.3:c.-149+2089C>T (IL19) MANE Select	ENSP00000499459.2:n.-149+2089C>T
ENST00000656872.2:c.-149+2337C>T (IL19)	ENSP00000499487.2:n.-149+2337C>T
ENST00000659065.1:c.-15+513G>A (IL10)	ENSP00000499588.1:n.-15+513G>A
ENST00000659642.1:c.-849G>A (IL10)	ENSP00000499509.1:n.-849G>A
ENST00000659997.2:c.-149+2089C>T (IL19)	ENSP00000499459.2:n.-149+2089C>T
ENST00000662320.1:n.67+2337C>T (IL19)
ENST00000664374.1:c.-14-835G>A (IL10)	ENSP00000499664.1:n.-14-835G>A
XM_011509506.1:c.-732G>A (IL10)	XP_011507808.1:n.-732G>A
NM_153758.3:c.-35+2089C>T (IL19)	NP_715639.1:n.-35+2089C>T
NM_001393490.1:c.-149+2337C>T (IL19)	NP_001380419.1:n.-149+2337C>T
NM_153758.5:c.-149+2089C>T (IL19) MANE Select	NP_715639.2:n.-149+2089C>T