Canonical Allele Identifier: CA2483128766
Gene: IL19 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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