Canonical Allele Identifier: CA36548047

Gene: IL10

Linked Data

• dbSNP Id: rs575853731
• gnomAD v2: 1-206942347-G-A
• gnomAD v3: 1-206769002-G-A
• gnomAD v4: 1-206769002-G-A
• MyVariant Identifiers: chr1:g.206942347G>A (hg19) ; chr1:g.206769002G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769002G>A , CM000663.2:g.206769002G>A	GRCh38
NC_000001.10:g.206942347G>A , CM000663.1:g.206942347G>A	GRCh37
NC_000001.9:g.205008970G>A	NCBI36
NG_012088.1:g.8493C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1176C>T
ENST00000471071.2:c.190-274C>T	ENSP00000493073.2:n.190-274C>T
ENST00000640756.2:n.255-274C>T
ENST00000659065.2:c.328-274C>T	ENSP00000499588.1:n.328-274C>T
ENST00000659642.2:c.328-274C>T	ENSP00000499509.1:n.328-274C>T
ENST00000664374.2:c.328-274C>T	ENSP00000499664.1:n.328-274C>T
ENST00000640756.1:n.244-274C>T
ENST00000659065.1:c.328-274C>T	ENSP00000499588.1:n.328-274C>T
ENST00000659642.1:c.328-274C>T	ENSP00000499509.1:n.328-274C>T
ENST00000664374.1:c.328-274C>T	ENSP00000499664.1:n.328-274C>T
ENST00000423557.1:c.445-274C>T MANE Select	ENSP00000412237.1:n.445-274C>T
ENST00000471071.1:n.360-274C>T
NM_000572.2:c.445-274C>T	NP_000563.1:n.445-274C>T
XM_011509506.1:c.445-274C>T	XP_011507808.1:n.445-274C>T
NM_000572.3:c.445-274C>T MANE Select	NP_000563.1:n.445-274C>T
NM_001382624.1:c.190-274C>T	NP_001369553.1:n.190-274C>T
NR_168466.1:n.742-274C>T
NR_168467.1:n.272-274C>T