Canonical Allele Identifier: CA344486404
Gene: IL19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206842620T>A , CM000663.2:g.206842620T>A GRCh38
NC_000001.10:g.207015965T>A , CM000663.1:g.207015965T>A GRCh37
NC_000001.9:g.205082588T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.532T>A MANE Select ENSP00000499459.2:p.Ter178Arg
ENST00000340758.7:c.532T>A ENSP00000343000.3:p.Ter178Arg
ENST00000656872.2:c.532T>A ENSP00000499487.2:p.Ter178Arg
ENST00000659997.2:c.532T>A ENSP00000499459.2:p.Ter178Arg
ENST00000270218.10:c.532T>A ENSP00000270218.6:p.Ter178Arg
ENST00000340758.6:c.646T>A ENSP00000343000.2:p.Ter216Arg
ENST00000620365.1:c.532T>A ENSP00000482668.1:p.Ter178Arg
NM_013371.3:c.532T>A NP_037503.2:p.Ter178Arg
NM_153758.2:c.646T>A NP_715639.1:p.Ter216Arg
XR_922482.1:n.202A>T
XR_922482.2:n.202A>T
NM_001369605.1:c.532T>A NP_001356534.1:p.Ter178Arg
NM_153758.3:c.646T>A NP_715639.1:p.Ter216Arg
NM_001393490.1:c.532T>A NP_001380419.1:p.Ter178Arg
NM_001393491.1:c.532T>A NP_001380420.1:p.Ter178Arg
NM_013371.5:c.532T>A NP_037503.2:p.Ter178Arg
NM_153758.5:c.532T>A MANE Select NP_715639.2:p.Ter178Arg