Canonical Allele Identifier: CA2573995255

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771284C>T , CM000663.2:g.206771284C>T	GRCh38
NC_000001.10:g.206944629C>T , CM000663.1:g.206944629C>T	GRCh37
NC_000001.9:g.205011252C>T	NCBI36
NG_012088.1:g.6211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.108+72G>A (IL10)	ENSP00000499588.1:n.108+72G>A
ENST00000659642.2:c.108+72G>A (IL10)	ENSP00000499509.1:n.108+72G>A
ENST00000664374.2:c.108+72G>A (IL10)	ENSP00000499664.1:n.108+72G>A
ENST00000659997.3:c.-149+206C>T (IL19) MANE Select	ENSP00000499459.2:n.-149+206C>T
ENST00000656872.2:c.-149+454C>T (IL19)	ENSP00000499487.2:n.-149+454C>T
ENST00000659065.1:c.108+72G>A (IL10)	ENSP00000499588.1:n.108+72G>A
ENST00000659642.1:c.108+72G>A (IL10)	ENSP00000499509.1:n.108+72G>A
ENST00000659997.2:c.-149+206C>T (IL19)	ENSP00000499459.2:n.-149+206C>T
ENST00000662320.1:n.67+454C>T (IL19)
ENST00000664374.1:c.108+72G>A (IL10)	ENSP00000499664.1:n.108+72G>A
ENST00000423557.1:c.225+72G>A (IL10) MANE Select	ENSP00000412237.1:n.225+72G>A
NM_000572.2:c.225+72G>A (IL10)	NP_000563.1:n.225+72G>A
XM_011509506.1:c.225+72G>A (IL10)	XP_011507808.1:n.225+72G>A
NM_000572.3:c.225+72G>A (IL10) MANE Select	NP_000563.1:n.225+72G>A
NM_153758.3:c.-35+206C>T (IL19)	NP_715639.1:n.-35+206C>T
NM_001393490.1:c.-149+454C>T (IL19)	NP_001380419.1:n.-149+454C>T
NM_153758.5:c.-149+206C>T (IL19) MANE Select	NP_715639.2:n.-149+206C>T
NR_168466.1:n.284+72G>A (IL10)