Canonical Allele Identifier: CA344482021

Gene: IL10 IL19

Linked Data

• MyVariant Identifiers: chr1:g.206944301T>G (hg19) ; chr1:g.206770956T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770956T>G , CM000663.2:g.206770956T>G	GRCh38
NC_000001.10:g.206944301T>G , CM000663.1:g.206944301T>G	GRCh37
NC_000001.9:g.205010924T>G	NCBI36
NG_012088.1:g.6539A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.234A>C (IL10)
ENST00000471071.2:c.74A>C (IL10)	ENSP00000493073.2:p.Asn25Thr
ENST00000659065.2:c.212A>C (IL10)	ENSP00000499588.1:p.Asn71Thr
ENST00000659642.2:c.212A>C (IL10)	ENSP00000499509.1:p.Asn71Thr
ENST00000664374.2:c.212A>C (IL10)	ENSP00000499664.1:p.Asn71Thr
ENST00000659997.3:c.-271T>G (IL19) MANE Select	ENSP00000499459.2:n.-271T>G
ENST00000656872.2:c.-149+126T>G (IL19)	ENSP00000499487.2:n.-149+126T>G
ENST00000659065.1:c.212A>C (IL10)	ENSP00000499588.1:p.Asn71Thr
ENST00000659642.1:c.212A>C (IL10)	ENSP00000499509.1:p.Asn71Thr
ENST00000659997.2:c.-271T>G (IL19)	ENSP00000499459.2:n.-271T>G
ENST00000662320.1:n.67+126T>G (IL19)
ENST00000664374.1:c.212A>C (IL10)	ENSP00000499664.1:p.Asn71Thr
ENST00000367099.3:n.234A>C (IL10)
ENST00000423557.1:c.329A>C (IL10) MANE Select	ENSP00000412237.1:p.Asn110Thr
ENST00000471071.1:n.244A>C (IL10)
NM_000572.2:c.329A>C (IL10)	NP_000563.1:p.Asn110Thr
XM_011509506.1:c.329A>C (IL10)	XP_011507808.1:p.Asn110Thr
NM_000572.3:c.329A>C (IL10) MANE Select	NP_000563.1:p.Asn110Thr
NM_153758.3:c.-157T>G (IL19)	NP_715639.1:n.-157T>G
NM_001382624.1:c.74A>C (IL10)	NP_001369553.1:p.Asn25Thr
NM_001393490.1:c.-149+126T>G (IL19)	NP_001380419.1:n.-149+126T>G
NM_153758.5:c.-271T>G (IL19) MANE Select	NP_715639.2:n.-271T>G
NR_168466.1:n.388A>C (IL10)