Canonical Allele Identifier: CA36554091
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs955850929

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776041A>G , CM000663.2:g.206776041A>G GRCh38
NC_000001.10:g.206949386A>G , CM000663.1:g.206949386A>G GRCh37
NC_000001.9:g.205016009A>G NCBI36
NG_012088.1:g.1454T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-149+4963A>G MANE Select ENSP00000499459.2:n.-149+4963A>G
ENST00000656872.2:c.-149+5211A>G ENSP00000499487.2:n.-149+5211A>G
ENST00000659997.2:c.-149+4963A>G ENSP00000499459.2:n.-149+4963A>G
ENST00000662320.1:n.67+5211A>G
NM_153758.3:c.-35+4963A>G NP_715639.1:n.-35+4963A>G
NM_001393490.1:c.-149+5211A>G NP_001380419.1:n.-149+5211A>G
NM_153758.5:c.-149+4963A>G MANE Select NP_715639.2:n.-149+4963A>G