Canonical Allele Identifier: CA36548046

Gene: IL10

Linked Data

• dbSNP Id: rs754838158
• gnomAD v2: 1-206942346-C-T
• gnomAD v3: 1-206769001-C-T
• gnomAD v4: 1-206769001-C-T
• MyVariant Identifiers: chr1:g.206942346C>T (hg19) ; chr1:g.206769001C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769001C>T , CM000663.2:g.206769001C>T	GRCh38
NC_000001.10:g.206942346C>T , CM000663.1:g.206942346C>T	GRCh37
NC_000001.9:g.205008969C>T	NCBI36
NG_012088.1:g.8494G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1177G>A
ENST00000471071.2:c.190-273G>A	ENSP00000493073.2:n.190-273G>A
ENST00000640756.2:n.255-273G>A
ENST00000659065.2:c.328-273G>A	ENSP00000499588.1:n.328-273G>A
ENST00000659642.2:c.328-273G>A	ENSP00000499509.1:n.328-273G>A
ENST00000664374.2:c.328-273G>A	ENSP00000499664.1:n.328-273G>A
ENST00000640756.1:n.244-273G>A
ENST00000659065.1:c.328-273G>A	ENSP00000499588.1:n.328-273G>A
ENST00000659642.1:c.328-273G>A	ENSP00000499509.1:n.328-273G>A
ENST00000664374.1:c.328-273G>A	ENSP00000499664.1:n.328-273G>A
ENST00000423557.1:c.445-273G>A MANE Select	ENSP00000412237.1:n.445-273G>A
ENST00000471071.1:n.360-273G>A
NM_000572.2:c.445-273G>A	NP_000563.1:n.445-273G>A
XM_011509506.1:c.445-273G>A	XP_011507808.1:n.445-273G>A
NM_000572.3:c.445-273G>A MANE Select	NP_000563.1:n.445-273G>A
NM_001382624.1:c.190-273G>A	NP_001369553.1:n.190-273G>A
NR_168466.1:n.742-273G>A
NR_168467.1:n.272-273G>A