Canonical Allele Identifier: CA2650218430

Gene: IL10 IL19

Linked Data

• gnomAD v4: 1-206770795-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770795G>T , CM000663.2:g.206770795G>T	GRCh38
NC_000001.10:g.206944140G>T , CM000663.1:g.206944140G>T	GRCh37
NC_000001.9:g.205010763G>T	NCBI36
NG_012088.1:g.6700C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+112C>A (IL10)
ENST00000471071.2:c.123+112C>A (IL10)	ENSP00000493073.2:n.123+112C>A
ENST00000659065.2:c.261+112C>A (IL10)	ENSP00000499588.1:n.261+112C>A
ENST00000659642.2:c.261+112C>A (IL10)	ENSP00000499509.1:n.261+112C>A
ENST00000664374.2:c.261+112C>A (IL10)	ENSP00000499664.1:n.261+112C>A
ENST00000659997.3:c.-432G>T (IL19) MANE Select	ENSP00000499459.2:n.-432G>T
ENST00000656872.2:c.-184G>T (IL19)	ENSP00000499487.2:n.-184G>T
ENST00000659065.1:c.261+112C>A (IL10)	ENSP00000499588.1:n.261+112C>A
ENST00000659642.1:c.261+112C>A (IL10)	ENSP00000499509.1:n.261+112C>A
ENST00000659997.2:c.-432G>T (IL19)	ENSP00000499459.2:n.-432G>T
ENST00000662320.1:n.32G>T (IL19)
ENST00000664374.1:c.261+112C>A (IL10)	ENSP00000499664.1:n.261+112C>A
ENST00000367099.3:n.283+112C>A (IL10)
ENST00000423557.1:c.378+112C>A (IL10) MANE Select	ENSP00000412237.1:n.378+112C>A
ENST00000471071.1:n.293+112C>A (IL10)
NM_000572.2:c.378+112C>A (IL10)	NP_000563.1:n.378+112C>A
XM_011509506.1:c.378+112C>A (IL10)	XP_011507808.1:n.378+112C>A
NM_000572.3:c.378+112C>A (IL10) MANE Select	NP_000563.1:n.378+112C>A
NM_153758.3:c.-318G>T (IL19)	NP_715639.1:n.-318G>T
NM_001382624.1:c.123+112C>A (IL10)	NP_001369553.1:n.123+112C>A
NM_001393490.1:c.-184G>T (IL19)	NP_001380419.1:n.-184G>T
NM_153758.5:c.-432G>T (IL19) MANE Select	NP_715639.2:n.-432G>T
NR_168466.1:n.437+112C>A (IL10)