Canonical Allele Identifier: CA36551351

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs776463142
• gnomAD v2: 1-206946308-C-A
• gnomAD v3: 1-206772963-C-A
• gnomAD v4: 1-206772963-C-A
• MyVariant Identifiers: chr1:g.206946308C>A (hg19) ; chr1:g.206772963C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772963C>A , CM000663.2:g.206772963C>A	GRCh38
NC_000001.10:g.206946308C>A , CM000663.1:g.206946308C>A	GRCh37
NC_000001.9:g.205012931C>A	NCBI36
NG_012088.1:g.4532G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-14-631G>T (IL10)	ENSP00000499588.1:n.-14-631G>T
ENST00000659642.2:c.-645G>T (IL10)	ENSP00000499509.1:n.-645G>T
ENST00000664374.2:c.-14-631G>T (IL10)	ENSP00000499664.1:n.-14-631G>T
ENST00000659997.3:c.-149+1885C>A (IL19) MANE Select	ENSP00000499459.2:n.-149+1885C>A
ENST00000656872.2:c.-149+2133C>A (IL19)	ENSP00000499487.2:n.-149+2133C>A
ENST00000659065.1:c.-14-631G>T (IL10)	ENSP00000499588.1:n.-14-631G>T
ENST00000659642.1:c.-645G>T (IL10)	ENSP00000499509.1:n.-645G>T
ENST00000659997.2:c.-149+1885C>A (IL19)	ENSP00000499459.2:n.-149+1885C>A
ENST00000662320.1:n.67+2133C>A (IL19)
ENST00000664374.1:c.-14-631G>T (IL10)	ENSP00000499664.1:n.-14-631G>T
XM_011509506.1:c.-528G>T (IL10)	XP_011507808.1:n.-528G>T
NM_153758.3:c.-35+1885C>A (IL19)	NP_715639.1:n.-35+1885C>A
NM_001393490.1:c.-149+2133C>A (IL19)	NP_001380419.1:n.-149+2133C>A
NM_153758.5:c.-149+1885C>A (IL19) MANE Select	NP_715639.2:n.-149+1885C>A