Canonical Allele Identifier: CA36551488

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs945107713
• gnomAD v3: 1-206773073-T-G
• gnomAD v4: 1-206773073-T-G
• MyVariant Identifiers: chr1:g.206946418T>G (hg19) ; chr1:g.206773073T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773073T>G , CM000663.2:g.206773073T>G	GRCh38
NC_000001.10:g.206946418T>G , CM000663.1:g.206946418T>G	GRCh37
NC_000001.9:g.205013041T>G	NCBI36
NG_012088.1:g.4422A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-15+607A>C (IL10)	ENSP00000499588.1:n.-15+607A>C
ENST00000659642.2:c.-755A>C (IL10)	ENSP00000499509.1:n.-755A>C
ENST00000664374.2:c.-14-741A>C (IL10)	ENSP00000499664.1:n.-14-741A>C
ENST00000659997.3:c.-149+1995T>G (IL19) MANE Select	ENSP00000499459.2:n.-149+1995T>G
ENST00000656872.2:c.-149+2243T>G (IL19)	ENSP00000499487.2:n.-149+2243T>G
ENST00000659065.1:c.-15+607A>C (IL10)	ENSP00000499588.1:n.-15+607A>C
ENST00000659642.1:c.-755A>C (IL10)	ENSP00000499509.1:n.-755A>C
ENST00000659997.2:c.-149+1995T>G (IL19)	ENSP00000499459.2:n.-149+1995T>G
ENST00000662320.1:n.67+2243T>G (IL19)
ENST00000664374.1:c.-14-741A>C (IL10)	ENSP00000499664.1:n.-14-741A>C
XM_011509506.1:c.-638A>C (IL10)	XP_011507808.1:n.-638A>C
NM_153758.3:c.-35+1995T>G (IL19)	NP_715639.1:n.-35+1995T>G
NM_001393490.1:c.-149+2243T>G (IL19)	NP_001380419.1:n.-149+2243T>G
NM_153758.5:c.-149+1995T>G (IL19) MANE Select	NP_715639.2:n.-149+1995T>G