Canonical Allele Identifier: CA2650218499

Gene: IL10 IL19

Linked Data

• gnomAD v4: 1-206770890-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770890A>G , CM000663.2:g.206770890A>G	GRCh38
NC_000001.10:g.206944235A>G , CM000663.1:g.206944235A>G	GRCh37
NC_000001.9:g.205010858A>G	NCBI36
NG_012088.1:g.6605T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+17T>C (IL10)
ENST00000471071.2:c.123+17T>C (IL10)	ENSP00000493073.2:n.123+17T>C
ENST00000659065.2:c.261+17T>C (IL10)	ENSP00000499588.1:n.261+17T>C
ENST00000659642.2:c.261+17T>C (IL10)	ENSP00000499509.1:n.261+17T>C
ENST00000664374.2:c.261+17T>C (IL10)	ENSP00000499664.1:n.261+17T>C
ENST00000659997.3:c.-337A>G (IL19) MANE Select	ENSP00000499459.2:n.-337A>G
ENST00000656872.2:c.-149+60A>G (IL19)	ENSP00000499487.2:n.-149+60A>G
ENST00000659065.1:c.261+17T>C (IL10)	ENSP00000499588.1:n.261+17T>C
ENST00000659642.1:c.261+17T>C (IL10)	ENSP00000499509.1:n.261+17T>C
ENST00000659997.2:c.-337A>G (IL19)	ENSP00000499459.2:n.-337A>G
ENST00000662320.1:n.67+60A>G (IL19)
ENST00000664374.1:c.261+17T>C (IL10)	ENSP00000499664.1:n.261+17T>C
ENST00000367099.3:n.283+17T>C (IL10)
ENST00000423557.1:c.378+17T>C (IL10) MANE Select	ENSP00000412237.1:n.378+17T>C
ENST00000471071.1:n.293+17T>C (IL10)
NM_000572.2:c.378+17T>C (IL10)	NP_000563.1:n.378+17T>C
XM_011509506.1:c.378+17T>C (IL10)	XP_011507808.1:n.378+17T>C
NM_000572.3:c.378+17T>C (IL10) MANE Select	NP_000563.1:n.378+17T>C
NM_153758.3:c.-223A>G (IL19)	NP_715639.1:n.-223A>G
NM_001382624.1:c.123+17T>C (IL10)	NP_001369553.1:n.123+17T>C
NM_001393490.1:c.-149+60A>G (IL19)	NP_001380419.1:n.-149+60A>G
NM_153758.5:c.-337A>G (IL19) MANE Select	NP_715639.2:n.-337A>G
NR_168466.1:n.437+17T>C (IL10)