Canonical Allele Identifier: CA2483128742
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs1674982063

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776035G>A , CM000663.2:g.206776035G>A GRCh38
NC_000001.10:g.206949380G>A , CM000663.1:g.206949380G>A GRCh37
NC_000001.9:g.205016003G>A NCBI36
NG_012088.1:g.1460C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-149+4957G>A MANE Select ENSP00000499459.2:n.-149+4957G>A
ENST00000656872.2:c.-149+5205G>A ENSP00000499487.2:n.-149+5205G>A
ENST00000659997.2:c.-149+4957G>A ENSP00000499459.2:n.-149+4957G>A
ENST00000662320.1:n.67+5205G>A
NM_153758.3:c.-35+4957G>A NP_715639.1:n.-35+4957G>A
NM_001393490.1:c.-149+5205G>A NP_001380419.1:n.-149+5205G>A
NM_153758.5:c.-149+4957G>A MANE Select NP_715639.2:n.-149+4957G>A