Canonical Allele Identifier: CA2747495003

Gene: IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206775971A>G , CM000663.2:g.206775971A>G	GRCh38
NC_000001.10:g.206949316A>G , CM000663.1:g.206949316A>G	GRCh37
NC_000001.9:g.205015939A>G	NCBI36
NG_012088.1:g.1524T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000659997.3:c.-149+4893A>G MANE Select	ENSP00000499459.2:n.-149+4893A>G
ENST00000656872.2:c.-149+5141A>G	ENSP00000499487.2:n.-149+5141A>G
ENST00000659997.2:c.-149+4893A>G	ENSP00000499459.2:n.-149+4893A>G
ENST00000662320.1:n.67+5141A>G
NM_153758.3:c.-35+4893A>G	NP_715639.1:n.-35+4893A>G
NM_001393490.1:c.-149+5141A>G	NP_001380419.1:n.-149+5141A>G
NM_153758.5:c.-149+4893A>G MANE Select	NP_715639.2:n.-149+4893A>G