Canonical Allele Identifier: CA528575014

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1246674717
• gnomAD v2: 1-206947124-G-A
• gnomAD v3: 1-206773779-G-A
• gnomAD v4: 1-206773779-G-A
• MyVariant Identifiers: chr1:g.206947124G>A (hg19) ; chr1:g.206773779G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773779G>A , CM000663.2:g.206773779G>A	GRCh38
NC_000001.10:g.206947124G>A , CM000663.1:g.206947124G>A	GRCh37
NC_000001.9:g.205013747G>A	NCBI36
NG_012088.1:g.3716C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-114C>T (IL10)	ENSP00000499588.1:n.-114C>T
ENST00000659642.2:c.-1118-343C>T (IL10)	ENSP00000499509.1:n.-1118-343C>T
ENST00000664374.2:c.-15+551C>T (IL10)	ENSP00000499664.1:n.-15+551C>T
ENST00000659997.3:c.-149+2701G>A (IL19) MANE Select	ENSP00000499459.2:n.-149+2701G>A
ENST00000656872.2:c.-149+2949G>A (IL19)	ENSP00000499487.2:n.-149+2949G>A
ENST00000659065.1:c.-114C>T (IL10)	ENSP00000499588.1:n.-114C>T
ENST00000659642.1:c.-1118-343C>T (IL10)	ENSP00000499509.1:n.-1118-343C>T
ENST00000659997.2:c.-149+2701G>A (IL19)	ENSP00000499459.2:n.-149+2701G>A
ENST00000662320.1:n.67+2949G>A (IL19)
ENST00000664374.1:c.-15+551C>T (IL10)	ENSP00000499664.1:n.-15+551C>T
XM_011509506.1:c.-1001-343C>T (IL10)	XP_011507808.1:n.-1001-343C>T
NM_153758.3:c.-35+2701G>A (IL19)	NP_715639.1:n.-35+2701G>A
NM_001393490.1:c.-149+2949G>A (IL19)	NP_001380419.1:n.-149+2949G>A
NM_153758.5:c.-149+2701G>A (IL19) MANE Select	NP_715639.2:n.-149+2701G>A