Canonical Allele Identifier: CA36554080

Gene: IL19

Linked Data

• dbSNP Id: rs966166488
• MyVariant Identifiers: chr1:g.206949379G>T (hg19) ; chr1:g.206776034G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206776034G>T , CM000663.2:g.206776034G>T	GRCh38
NC_000001.10:g.206949379G>T , CM000663.1:g.206949379G>T	GRCh37
NC_000001.9:g.205016002G>T	NCBI36
NG_012088.1:g.1461C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000659997.3:c.-149+4956G>T MANE Select	ENSP00000499459.2:n.-149+4956G>T
ENST00000656872.2:c.-149+5204G>T	ENSP00000499487.2:n.-149+5204G>T
ENST00000659997.2:c.-149+4956G>T	ENSP00000499459.2:n.-149+4956G>T
ENST00000662320.1:n.67+5204G>T
NM_153758.3:c.-35+4956G>T	NP_715639.1:n.-35+4956G>T
NM_001393490.1:c.-149+5204G>T	NP_001380419.1:n.-149+5204G>T
NM_153758.5:c.-149+4956G>T MANE Select	NP_715639.2:n.-149+4956G>T