Canonical Allele Identifier: CA2483133719
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs880790
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206786871C>A , CM000663.2:g.206786871C>A GRCh38
NC_000001.10:g.206960216C>A , CM000663.1:g.206960216C>A GRCh37
NC_000001.9:g.205026839C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-148-11990C>A MANE Select ENSP00000499459.2:n.-148-11990C>A
ENST00000656872.2:c.-148-11990C>A ENSP00000499487.2:n.-148-11990C>A
ENST00000659997.2:c.-148-11990C>A ENSP00000499459.2:n.-148-11990C>A
ENST00000662320.1:n.68-11990C>A
NM_153758.3:c.-34-11990C>A NP_715639.1:n.-34-11990C>A
NM_001393490.1:c.-148-11990C>A NP_001380419.1:n.-148-11990C>A
NM_153758.5:c.-148-11990C>A MANE Select NP_715639.2:n.-148-11990C>A
Search 100 bp 5'
Search 100 bp 3'