Canonical Allele Identifier: CA1011578833

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1674899528
• gnomAD v3: 1-206773060-A-G
• gnomAD v4: 1-206773060-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773060A>G , CM000663.2:g.206773060A>G	GRCh38
NC_000001.10:g.206946405A>G , CM000663.1:g.206946405A>G	GRCh37
NC_000001.9:g.205013028A>G	NCBI36
NG_012088.1:g.4435T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+620T>C (IL10)	ENSP00000499588.1:n.-15+620T>C
ENST00000659642.2:c.-742T>C (IL10)	ENSP00000499509.1:n.-742T>C
ENST00000664374.2:c.-14-728T>C (IL10)	ENSP00000499664.1:n.-14-728T>C
ENST00000659997.3:c.-149+1982A>G (IL19) MANE Select	ENSP00000499459.2:n.-149+1982A>G
ENST00000656872.2:c.-149+2230A>G (IL19)	ENSP00000499487.2:n.-149+2230A>G
ENST00000659065.1:c.-15+620T>C (IL10)	ENSP00000499588.1:n.-15+620T>C
ENST00000659642.1:c.-742T>C (IL10)	ENSP00000499509.1:n.-742T>C
ENST00000659997.2:c.-149+1982A>G (IL19)	ENSP00000499459.2:n.-149+1982A>G
ENST00000662320.1:n.67+2230A>G (IL19)
ENST00000664374.1:c.-14-728T>C (IL10)	ENSP00000499664.1:n.-14-728T>C
XM_011509506.1:c.-625T>C (IL10)	XP_011507808.1:n.-625T>C
NM_153758.3:c.-35+1982A>G (IL19)	NP_715639.1:n.-35+1982A>G
NM_001393490.1:c.-149+2230A>G (IL19)	NP_001380419.1:n.-149+2230A>G
NM_153758.5:c.-149+1982A>G (IL19) MANE Select	NP_715639.2:n.-149+1982A>G