Canonical Allele Identifier: CA2560895857
Gene: IL19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776027C>A , CM000663.2:g.206776027C>A GRCh38
NC_000001.10:g.206949372C>A , CM000663.1:g.206949372C>A GRCh37
NC_000001.9:g.205015995C>A NCBI36
NG_012088.1:g.1468G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-149+4949C>A MANE Select ENSP00000499459.2:n.-149+4949C>A
ENST00000656872.2:c.-149+5197C>A ENSP00000499487.2:n.-149+5197C>A
ENST00000659997.2:c.-149+4949C>A ENSP00000499459.2:n.-149+4949C>A
ENST00000662320.1:n.67+5197C>A
NM_153758.3:c.-35+4949C>A NP_715639.1:n.-35+4949C>A
NM_001393490.1:c.-149+5197C>A NP_001380419.1:n.-149+5197C>A
NM_153758.5:c.-149+4949C>A MANE Select NP_715639.2:n.-149+4949C>A