Canonical Allele Identifier: CA730541126
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs1248847898
gnomAD v3: 1-206776036-G-A
gnomAD v4: 1-206776036-G-A
MyVariant Identifiers: chr1:g.206949381G>A (hg19) chr1:g.206776036G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776036G>A , CM000663.2:g.206776036G>A GRCh38
NC_000001.10:g.206949381G>A , CM000663.1:g.206949381G>A GRCh37
NC_000001.9:g.205016004G>A NCBI36
NG_012088.1:g.1459C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-149+4958G>A MANE Select ENSP00000499459.2:n.-149+4958G>A
ENST00000656872.2:c.-149+5206G>A ENSP00000499487.2:n.-149+5206G>A
ENST00000659997.2:c.-149+4958G>A ENSP00000499459.2:n.-149+4958G>A
ENST00000662320.1:n.67+5206G>A
NM_153758.3:c.-35+4958G>A NP_715639.1:n.-35+4958G>A
NM_001393490.1:c.-149+5206G>A NP_001380419.1:n.-149+5206G>A
NM_153758.5:c.-149+4958G>A MANE Select NP_715639.2:n.-149+4958G>A
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