Canonical Allele Identifier: CA2740217893

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773097T>C , CM000663.2:g.206773097T>C	GRCh38
NC_000001.10:g.206946442T>C , CM000663.1:g.206946442T>C	GRCh37
NC_000001.9:g.205013065T>C	NCBI36
NG_012088.1:g.4398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+583A>G (IL10)	ENSP00000499588.1:n.-15+583A>G
ENST00000659642.2:c.-779A>G (IL10)	ENSP00000499509.1:n.-779A>G
ENST00000664374.2:c.-14-765A>G (IL10)	ENSP00000499664.1:n.-14-765A>G
ENST00000659997.3:c.-149+2019T>C (IL19) MANE Select	ENSP00000499459.2:n.-149+2019T>C
ENST00000656872.2:c.-149+2267T>C (IL19)	ENSP00000499487.2:n.-149+2267T>C
ENST00000659065.1:c.-15+583A>G (IL10)	ENSP00000499588.1:n.-15+583A>G
ENST00000659642.1:c.-779A>G (IL10)	ENSP00000499509.1:n.-779A>G
ENST00000659997.2:c.-149+2019T>C (IL19)	ENSP00000499459.2:n.-149+2019T>C
ENST00000662320.1:n.67+2267T>C (IL19)
ENST00000664374.1:c.-14-765A>G (IL10)	ENSP00000499664.1:n.-14-765A>G
XM_011509506.1:c.-662A>G (IL10)	XP_011507808.1:n.-662A>G
NM_153758.3:c.-35+2019T>C (IL19)	NP_715639.1:n.-35+2019T>C
NM_001393490.1:c.-149+2267T>C (IL19)	NP_001380419.1:n.-149+2267T>C
NM_153758.5:c.-149+2019T>C (IL19) MANE Select	NP_715639.2:n.-149+2019T>C