Canonical Allele Identifier: CA36554044
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs35101374
gnomAD v2: 1-206949334-T-C
gnomAD v3: 1-206775989-T-C
gnomAD v4: 1-206775989-T-C
MyVariant Identifiers: chr1:g.206949334T>C (hg19) chr1:g.206775989T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206775989T>C , CM000663.2:g.206775989T>C GRCh38
NC_000001.10:g.206949334T>C , CM000663.1:g.206949334T>C GRCh37
NC_000001.9:g.205015957T>C NCBI36
NG_012088.1:g.1506A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.-149+4911T>C MANE Select ENSP00000499459.2:n.-149+4911T>C
ENST00000656872.2:c.-149+5159T>C ENSP00000499487.2:n.-149+5159T>C
ENST00000659997.2:c.-149+4911T>C ENSP00000499459.2:n.-149+4911T>C
ENST00000662320.1:n.67+5159T>C
NM_153758.3:c.-35+4911T>C NP_715639.1:n.-35+4911T>C
NM_001393490.1:c.-149+5159T>C NP_001380419.1:n.-149+5159T>C
NM_153758.5:c.-149+4911T>C MANE Select NP_715639.2:n.-149+4911T>C
Search 100 bp 5'
Search 100 bp 3'