Canonical Allele Identifier: CA2580581877

Gene: IL10 IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773127C>G , CM000663.2:g.206773127C>G	GRCh38
NC_000001.10:g.206946472C>G , CM000663.1:g.206946472C>G	GRCh37
NC_000001.9:g.205013095C>G	NCBI36
NG_012088.1:g.4368G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+553G>C (IL10)	ENSP00000499588.1:n.-15+553G>C
ENST00000659642.2:c.-809G>C (IL10)	ENSP00000499509.1:n.-809G>C
ENST00000664374.2:c.-14-795G>C (IL10)	ENSP00000499664.1:n.-14-795G>C
ENST00000659997.3:c.-149+2049C>G (IL19) MANE Select	ENSP00000499459.2:n.-149+2049C>G
ENST00000656872.2:c.-149+2297C>G (IL19)	ENSP00000499487.2:n.-149+2297C>G
ENST00000659065.1:c.-15+553G>C (IL10)	ENSP00000499588.1:n.-15+553G>C
ENST00000659642.1:c.-809G>C (IL10)	ENSP00000499509.1:n.-809G>C
ENST00000659997.2:c.-149+2049C>G (IL19)	ENSP00000499459.2:n.-149+2049C>G
ENST00000662320.1:n.67+2297C>G (IL19)
ENST00000664374.1:c.-14-795G>C (IL10)	ENSP00000499664.1:n.-14-795G>C
XM_011509506.1:c.-692G>C (IL10)	XP_011507808.1:n.-692G>C
NM_153758.3:c.-35+2049C>G (IL19)	NP_715639.1:n.-35+2049C>G
NM_001393490.1:c.-149+2297C>G (IL19)	NP_001380419.1:n.-149+2297C>G
NM_153758.5:c.-149+2049C>G (IL19) MANE Select	NP_715639.2:n.-149+2049C>G