Canonical Allele Identifier: CA2650218579

Gene: IL10 IL19

Linked Data

• gnomAD v4: 1-206771190-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771190G>T , CM000663.2:g.206771190G>T	GRCh38
NC_000001.10:g.206944535G>T , CM000663.1:g.206944535G>T	GRCh37
NC_000001.9:g.205011158G>T	NCBI36
NG_012088.1:g.6305C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471071.2:c.-161C>A (IL10)	ENSP00000493073.2:n.-161C>A
ENST00000659065.2:c.109-131C>A (IL10)	ENSP00000499588.1:n.109-131C>A
ENST00000659642.2:c.109-131C>A (IL10)	ENSP00000499509.1:n.109-131C>A
ENST00000664374.2:c.109-131C>A (IL10)	ENSP00000499664.1:n.109-131C>A
ENST00000659997.3:c.-149+112G>T (IL19) MANE Select	ENSP00000499459.2:n.-149+112G>T
ENST00000656872.2:c.-149+360G>T (IL19)	ENSP00000499487.2:n.-149+360G>T
ENST00000659065.1:c.109-131C>A (IL10)	ENSP00000499588.1:n.109-131C>A
ENST00000659642.1:c.109-131C>A (IL10)	ENSP00000499509.1:n.109-131C>A
ENST00000659997.2:c.-149+112G>T (IL19)	ENSP00000499459.2:n.-149+112G>T
ENST00000662320.1:n.67+360G>T (IL19)
ENST00000664374.1:c.109-131C>A (IL10)	ENSP00000499664.1:n.109-131C>A
ENST00000423557.1:c.226-131C>A (IL10) MANE Select	ENSP00000412237.1:n.226-131C>A
ENST00000471071.1:n.10C>A (IL10)
NM_000572.2:c.226-131C>A (IL10)	NP_000563.1:n.226-131C>A
XM_011509506.1:c.226-131C>A (IL10)	XP_011507808.1:n.226-131C>A
NM_000572.3:c.226-131C>A (IL10) MANE Select	NP_000563.1:n.226-131C>A
NM_153758.3:c.-35+112G>T (IL19)	NP_715639.1:n.-35+112G>T
NM_001393490.1:c.-149+360G>T (IL19)	NP_001380419.1:n.-149+360G>T
NM_153758.5:c.-149+112G>T (IL19) MANE Select	NP_715639.2:n.-149+112G>T
NR_168466.1:n.285-131C>A (IL10)