Canonical Allele Identifier: CA36554085
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs530424802
gnomAD v2: 1-206949383-T-A
gnomAD v3: 1-206776038-T-A
gnomAD v4: 1-206776038-T-A
MyVariant Identifiers: chr1:g.206949383T>A (hg19) chr1:g.206776038T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776038T>A , CM000663.2:g.206776038T>A GRCh38
NC_000001.10:g.206949383T>A , CM000663.1:g.206949383T>A GRCh37
NC_000001.9:g.205016006T>A NCBI36
NG_012088.1:g.1457A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-149+4960T>A MANE Select ENSP00000499459.2:n.-149+4960T>A
ENST00000656872.2:c.-149+5208T>A ENSP00000499487.2:n.-149+5208T>A
ENST00000659997.2:c.-149+4960T>A ENSP00000499459.2:n.-149+4960T>A
ENST00000662320.1:n.67+5208T>A
NM_153758.3:c.-35+4960T>A NP_715639.1:n.-35+4960T>A
NM_001393490.1:c.-149+5208T>A NP_001380419.1:n.-149+5208T>A
NM_153758.5:c.-149+4960T>A MANE Select NP_715639.2:n.-149+4960T>A
Search 100 bp 5'
Search 100 bp 3'