Canonical Allele Identifier: CA1363765

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs771912629
• ExAC: 1:206944257 G / T
• gnomAD v2: 1-206944257-G-T
• gnomAD v3: 1-206770912-G-T
• gnomAD v4: 1-206770912-G-T
• MyVariant Identifiers: chr1:g.206944257G>T (hg19) ; chr1:g.206770912G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770912G>T , CM000663.2:g.206770912G>T	GRCh38
NC_000001.10:g.206944257G>T , CM000663.1:g.206944257G>T	GRCh37
NC_000001.9:g.205010880G>T	NCBI36
NG_012088.1:g.6583C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.278C>A (IL10)
ENST00000471071.2:c.118C>A (IL10)	ENSP00000493073.2:p.Arg40Ser
ENST00000659065.2:c.256C>A (IL10)	ENSP00000499588.1:p.Arg86Ser
ENST00000659642.2:c.256C>A (IL10)	ENSP00000499509.1:p.Arg86Ser
ENST00000664374.2:c.256C>A (IL10)	ENSP00000499664.1:p.Arg86Ser
ENST00000659997.3:c.-315G>T (IL19) MANE Select	ENSP00000499459.2:n.-315G>T
ENST00000656872.2:c.-149+82G>T (IL19)	ENSP00000499487.2:n.-149+82G>T
ENST00000659065.1:c.256C>A (IL10)	ENSP00000499588.1:p.Arg86Ser
ENST00000659642.1:c.256C>A (IL10)	ENSP00000499509.1:p.Arg86Ser
ENST00000659997.2:c.-315G>T (IL19)	ENSP00000499459.2:n.-315G>T
ENST00000662320.1:n.67+82G>T (IL19)
ENST00000664374.1:c.256C>A (IL10)	ENSP00000499664.1:p.Arg86Ser
ENST00000367099.3:n.278C>A (IL10)
ENST00000423557.1:c.373C>A (IL10) MANE Select	ENSP00000412237.1:p.Arg125Ser
ENST00000471071.1:n.288C>A (IL10)
NM_000572.2:c.373C>A (IL10)	NP_000563.1:p.Arg125Ser
XM_011509506.1:c.373C>A (IL10)	XP_011507808.1:p.Arg125Ser
NM_000572.3:c.373C>A (IL10) MANE Select	NP_000563.1:p.Arg125Ser
NM_153758.3:c.-201G>T (IL19)	NP_715639.1:n.-201G>T
NM_001382624.1:c.118C>A (IL10)	NP_001369553.1:p.Arg40Ser
NM_001393490.1:c.-149+82G>T (IL19)	NP_001380419.1:n.-149+82G>T
NM_153758.5:c.-315G>T (IL19) MANE Select	NP_715639.2:n.-315G>T
NR_168466.1:n.432C>A (IL10)