Canonical Allele Identifier: CA36552000

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs751479957
• MyVariant Identifiers: chr1:g.206947107C>T (hg19) ; chr1:g.206773762C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773762C>T , CM000663.2:g.206773762C>T	GRCh38
NC_000001.10:g.206947107C>T , CM000663.1:g.206947107C>T	GRCh37
NC_000001.9:g.205013730C>T	NCBI36
NG_012088.1:g.3733G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-97G>A (IL10)	ENSP00000499588.1:n.-97G>A
ENST00000659642.2:c.-1118-326G>A (IL10)	ENSP00000499509.1:n.-1118-326G>A
ENST00000664374.2:c.-15+568G>A (IL10)	ENSP00000499664.1:n.-15+568G>A
ENST00000659997.3:c.-149+2684C>T (IL19) MANE Select	ENSP00000499459.2:n.-149+2684C>T
ENST00000656872.2:c.-149+2932C>T (IL19)	ENSP00000499487.2:n.-149+2932C>T
ENST00000659065.1:c.-97G>A (IL10)	ENSP00000499588.1:n.-97G>A
ENST00000659642.1:c.-1118-326G>A (IL10)	ENSP00000499509.1:n.-1118-326G>A
ENST00000659997.2:c.-149+2684C>T (IL19)	ENSP00000499459.2:n.-149+2684C>T
ENST00000662320.1:n.67+2932C>T (IL19)
ENST00000664374.1:c.-15+568G>A (IL10)	ENSP00000499664.1:n.-15+568G>A
XM_011509506.1:c.-1001-326G>A (IL10)	XP_011507808.1:n.-1001-326G>A
NM_153758.3:c.-35+2684C>T (IL19)	NP_715639.1:n.-35+2684C>T
NM_001393490.1:c.-149+2932C>T (IL19)	NP_001380419.1:n.-149+2932C>T
NM_153758.5:c.-149+2684C>T (IL19) MANE Select	NP_715639.2:n.-149+2684C>T