Canonical Allele Identifier: CA15106931
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs61815643
gnomAD v2: 1-206956116-G-T
gnomAD v3: 1-206782771-G-T
gnomAD v4: 1-206782771-G-T
MyVariant Identifiers: chr1:g.206956116G>T (hg19) chr1:g.206782771G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206782771G>T , CM000663.2:g.206782771G>T GRCh38
NC_000001.10:g.206956116G>T , CM000663.1:g.206956116G>T GRCh37
NC_000001.9:g.205022739G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.-149+11693G>T MANE Select ENSP00000499459.2:n.-149+11693G>T
ENST00000656872.2:c.-149+11941G>T ENSP00000499487.2:n.-149+11941G>T
ENST00000659997.2:c.-149+11693G>T ENSP00000499459.2:n.-149+11693G>T
ENST00000662320.1:n.67+11941G>T
NM_153758.3:c.-35+11693G>T NP_715639.1:n.-35+11693G>T
NM_001393490.1:c.-149+11941G>T NP_001380419.1:n.-149+11941G>T
NM_153758.5:c.-149+11693G>T MANE Select NP_715639.2:n.-149+11693G>T
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