Canonical Allele Identifier: CA36578495
Gene: IL19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206809585A>C , CM000663.2:g.206809585A>C GRCh38
NC_000001.10:g.206982930A>C , CM000663.1:g.206982930A>C GRCh37
NC_000001.9:g.205049553A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.-3+10579A>C MANE Select ENSP00000499459.2:n.-3+10579A>C
ENST00000656872.2:c.-3+10579A>C ENSP00000499487.2:n.-3+10579A>C
ENST00000659997.2:c.-3+10579A>C ENSP00000499459.2:n.-3+10579A>C
ENST00000662320.1:n.213+10579A>C
ENST00000340758.6:c.112+10579A>C ENSP00000343000.2:n.112+10579A>C
NM_153758.2:c.112+10579A>C NP_715639.1:n.112+10579A>C
NM_153758.3:c.112+10579A>C NP_715639.1:n.112+10579A>C
NM_001393490.1:c.-3+10579A>C NP_001380419.1:n.-3+10579A>C
NM_153758.5:c.-3+10579A>C MANE Select NP_715639.2:n.-3+10579A>C
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