Canonical Allele Identifier: CA730538454

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1251969920
• MyVariant Identifiers: chr1:g.206944989T>C (hg19) ; chr1:g.206771644T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206771644T>C , CM000663.2:g.206771644T>C	GRCh38
NC_000001.10:g.206944989T>C , CM000663.1:g.206944989T>C	GRCh37
NC_000001.9:g.205011612T>C	NCBI36
NG_012088.1:g.5851A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.49-229A>G (IL10)	ENSP00000499588.1:n.49-229A>G
ENST00000659642.2:c.49-229A>G (IL10)	ENSP00000499509.1:n.49-229A>G
ENST00000664374.2:c.49-229A>G (IL10)	ENSP00000499664.1:n.49-229A>G
ENST00000659997.3:c.-149+566T>C (IL19) MANE Select	ENSP00000499459.2:n.-149+566T>C
ENST00000656872.2:c.-149+814T>C (IL19)	ENSP00000499487.2:n.-149+814T>C
ENST00000659065.1:c.49-229A>G (IL10)	ENSP00000499588.1:n.49-229A>G
ENST00000659642.1:c.49-229A>G (IL10)	ENSP00000499509.1:n.49-229A>G
ENST00000659997.2:c.-149+566T>C (IL19)	ENSP00000499459.2:n.-149+566T>C
ENST00000662320.1:n.67+814T>C (IL19)
ENST00000664374.1:c.49-229A>G (IL10)	ENSP00000499664.1:n.49-229A>G
ENST00000423557.1:c.166-229A>G (IL10) MANE Select	ENSP00000412237.1:n.166-229A>G
NM_000572.2:c.166-229A>G (IL10)	NP_000563.1:n.166-229A>G
XM_011509506.1:c.166-229A>G (IL10)	XP_011507808.1:n.166-229A>G
NM_000572.3:c.166-229A>G (IL10) MANE Select	NP_000563.1:n.166-229A>G
NM_153758.3:c.-35+566T>C (IL19)	NP_715639.1:n.-35+566T>C
NM_001393490.1:c.-149+814T>C (IL19)	NP_001380419.1:n.-149+814T>C
NM_153758.5:c.-149+566T>C (IL19) MANE Select	NP_715639.2:n.-149+566T>C
NR_168466.1:n.225-229A>G (IL10)