Canonical Allele Identifier: CA730537555

Gene: IL10

Linked Data

• dbSNP Id: rs1359037064
• gnomAD v3: 1-206770737-G-A
• gnomAD v4: 1-206770737-G-A
• MyVariant Identifiers: chr1:g.206944082G>A (hg19) ; chr1:g.206770737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770737G>A , CM000663.2:g.206770737G>A	GRCh38
NC_000001.10:g.206944082G>A , CM000663.1:g.206944082G>A	GRCh37
NC_000001.9:g.205010705G>A	NCBI36
NG_012088.1:g.6758C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+170C>T
ENST00000471071.2:c.123+170C>T	ENSP00000493073.2:n.123+170C>T
ENST00000659065.2:c.261+170C>T	ENSP00000499588.1:n.261+170C>T
ENST00000659642.2:c.261+170C>T	ENSP00000499509.1:n.261+170C>T
ENST00000664374.2:c.261+170C>T	ENSP00000499664.1:n.261+170C>T
ENST00000659065.1:c.261+170C>T	ENSP00000499588.1:n.261+170C>T
ENST00000659642.1:c.261+170C>T	ENSP00000499509.1:n.261+170C>T
ENST00000664374.1:c.261+170C>T	ENSP00000499664.1:n.261+170C>T
ENST00000367099.3:n.283+170C>T
ENST00000423557.1:c.378+170C>T MANE Select	ENSP00000412237.1:n.378+170C>T
ENST00000471071.1:n.293+170C>T
NM_000572.2:c.378+170C>T	NP_000563.1:n.378+170C>T
XM_011509506.1:c.378+170C>T	XP_011507808.1:n.378+170C>T
NM_000572.3:c.378+170C>T MANE Select	NP_000563.1:n.378+170C>T
NM_001382624.1:c.123+170C>T	NP_001369553.1:n.123+170C>T
NR_168466.1:n.437+170C>T