Canonical Allele Identifier: CA730539443

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs1426577442
• gnomAD v3: 1-206773041-C-T
• gnomAD v4: 1-206773041-C-T
• MyVariant Identifiers: chr1:g.206946386C>T (hg19) ; chr1:g.206773041C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773041C>T , CM000663.2:g.206773041C>T	GRCh38
NC_000001.10:g.206946386C>T , CM000663.1:g.206946386C>T	GRCh37
NC_000001.9:g.205013009C>T	NCBI36
NG_012088.1:g.4454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659065.2:c.-15+639G>A (IL10)	ENSP00000499588.1:n.-15+639G>A
ENST00000659642.2:c.-723G>A (IL10)	ENSP00000499509.1:n.-723G>A
ENST00000664374.2:c.-14-709G>A (IL10)	ENSP00000499664.1:n.-14-709G>A
ENST00000659997.3:c.-149+1963C>T (IL19) MANE Select	ENSP00000499459.2:n.-149+1963C>T
ENST00000656872.2:c.-149+2211C>T (IL19)	ENSP00000499487.2:n.-149+2211C>T
ENST00000659065.1:c.-15+639G>A (IL10)	ENSP00000499588.1:n.-15+639G>A
ENST00000659642.1:c.-723G>A (IL10)	ENSP00000499509.1:n.-723G>A
ENST00000659997.2:c.-149+1963C>T (IL19)	ENSP00000499459.2:n.-149+1963C>T
ENST00000662320.1:n.67+2211C>T (IL19)
ENST00000664374.1:c.-14-709G>A (IL10)	ENSP00000499664.1:n.-14-709G>A
XM_011509506.1:c.-606G>A (IL10)	XP_011507808.1:n.-606G>A
NM_153758.3:c.-35+1963C>T (IL19)	NP_715639.1:n.-35+1963C>T
NM_001393490.1:c.-149+2211C>T (IL19)	NP_001380419.1:n.-149+2211C>T
NM_153758.5:c.-149+1963C>T (IL19) MANE Select	NP_715639.2:n.-149+1963C>T