Canonical Allele Identifier: CA2697949907

Gene: IL19

Linked Data

• dbSNP Id: rs2102444090

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206776005T>C , CM000663.2:g.206776005T>C	GRCh38
NC_000001.10:g.206949350T>C , CM000663.1:g.206949350T>C	GRCh37
NC_000001.9:g.205015973T>C	NCBI36
NG_012088.1:g.1490A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000659997.3:c.-149+4927T>C MANE Select	ENSP00000499459.2:n.-149+4927T>C
ENST00000656872.2:c.-149+5175T>C	ENSP00000499487.2:n.-149+5175T>C
ENST00000659997.2:c.-149+4927T>C	ENSP00000499459.2:n.-149+4927T>C
ENST00000662320.1:n.67+5175T>C
NM_153758.3:c.-35+4927T>C	NP_715639.1:n.-35+4927T>C
NM_001393490.1:c.-149+5175T>C	NP_001380419.1:n.-149+5175T>C
NM_153758.5:c.-149+4927T>C MANE Select	NP_715639.2:n.-149+4927T>C