Canonical Allele Identifier: CA36554102

Gene: IL19

Linked Data

• dbSNP Id: rs969043350
• gnomAD v3: 1-206776078-C-G
• gnomAD v4: 1-206776078-C-G
• MyVariant Identifiers: chr1:g.206949423C>G (hg19) ; chr1:g.206776078C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206776078C>G , CM000663.2:g.206776078C>G	GRCh38
NC_000001.10:g.206949423C>G , CM000663.1:g.206949423C>G	GRCh37
NC_000001.9:g.205016046C>G	NCBI36
NG_012088.1:g.1417G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000659997.3:c.-149+5000C>G MANE Select	ENSP00000499459.2:n.-149+5000C>G
ENST00000656872.2:c.-149+5248C>G	ENSP00000499487.2:n.-149+5248C>G
ENST00000659997.2:c.-149+5000C>G	ENSP00000499459.2:n.-149+5000C>G
ENST00000662320.1:n.67+5248C>G
NM_153758.3:c.-35+5000C>G	NP_715639.1:n.-35+5000C>G
NM_001393490.1:c.-149+5248C>G	NP_001380419.1:n.-149+5248C>G
NM_153758.5:c.-149+5000C>G MANE Select	NP_715639.2:n.-149+5000C>G