Canonical Allele Identifier: CA1363853

Gene: IL10 IL19

Linked Data

• ClinVar Variation Id: 456662
• ClinVar RCV Id: RCV000767995 ; RCV001257069 ; RCV003224318
• dbSNP Id: rs145922845
• ExAC: 1:206945738 C / T
• gnomAD v2: 1-206945738-C-T
• gnomAD v3: 1-206772393-C-T
• gnomAD v4: 1-206772393-C-T
• MyVariant Identifiers: chr1:g.206945738C>T (hg19) ; chr1:g.206772393C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206772393C>T , CM000663.2:g.206772393C>T	GRCh38
NC_000001.10:g.206945738C>T , CM000663.1:g.206945738C>T	GRCh37
NC_000001.9:g.205012361C>T	NCBI36
NG_012088.1:g.5102G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-14-61G>A (IL10)	ENSP00000499588.1:n.-14-61G>A
ENST00000659642.2:c.-75G>A (IL10)	ENSP00000499509.1:n.-75G>A
ENST00000664374.2:c.-14-61G>A (IL10)	ENSP00000499664.1:n.-14-61G>A
ENST00000659997.3:c.-149+1315C>T (IL19) MANE Select	ENSP00000499459.2:n.-149+1315C>T
ENST00000656872.2:c.-149+1563C>T (IL19)	ENSP00000499487.2:n.-149+1563C>T
ENST00000659065.1:c.-14-61G>A (IL10)	ENSP00000499588.1:n.-14-61G>A
ENST00000659642.1:c.-75G>A (IL10)	ENSP00000499509.1:n.-75G>A
ENST00000659997.2:c.-149+1315C>T (IL19)	ENSP00000499459.2:n.-149+1315C>T
ENST00000662320.1:n.67+1563C>T (IL19)
ENST00000664374.1:c.-14-61G>A (IL10)	ENSP00000499664.1:n.-14-61G>A
ENST00000423557.1:c.43G>A (IL10) MANE Select	ENSP00000412237.1:p.Gly15Arg
NM_000572.2:c.43G>A (IL10)	NP_000563.1:p.Gly15Arg
XM_011509506.1:c.43G>A (IL10)	XP_011507808.1:p.Gly15Arg
NM_000572.3:c.43G>A (IL10) MANE Select	NP_000563.1:p.Gly15Arg
NM_153758.3:c.-35+1315C>T (IL19)	NP_715639.1:n.-35+1315C>T
NM_001393490.1:c.-149+1563C>T (IL19)	NP_001380419.1:n.-149+1563C>T
NM_153758.5:c.-149+1315C>T (IL19) MANE Select	NP_715639.2:n.-149+1315C>T
NR_168466.1:n.102G>A (IL10)