Canonical Allele Identifier: CA528577113
Gene: IL19 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.206841127A>T
GRCh37 chr1:g.207014472A>T
gnomAD v2:
1:207014472 A / T
gnomAD v3:
1:206841127 A / T
gnomAD v4:
chr1-206841127-A-T
Joint Max Group AF 0.00001438 (NFE)
Genomes Max Group AF 0.00001972 (NFE)
Exomes Max Group AF 0.00001218 (NFE)
dbSNP:
2243188
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206841127A>T , CM000663.2:g.206841127A>T GRCh38
NC_000001.10:g.207014472A>T , CM000663.1:g.207014472A>T GRCh37
NC_000001.9:g.205081095A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.438+49A>T MANE Select ENSP00000499459.2:n.438+49A>T
ENST00000340758.7:c.438+49A>T ENSP00000343000.3:n.438+49A>T
ENST00000656872.2:c.438+49A>T ENSP00000499487.2:n.438+49A>T
ENST00000659997.2:c.438+49A>T ENSP00000499459.2:n.438+49A>T
ENST00000270218.10:c.438+49A>T ENSP00000270218.6:n.438+49A>T
ENST00000340758.6:c.552+49A>T ENSP00000343000.2:n.552+49A>T
ENST00000620365.1:c.438+49A>T ENSP00000482668.1:n.438+49A>T
NM_013371.3:c.438+49A>T NP_037503.2:n.438+49A>T
NM_153758.2:c.552+49A>T NP_715639.1:n.552+49A>T
XR_922482.1:n.701T>A
XR_922482.2:n.701T>A
NM_001369605.1:c.438+49A>T NP_001356534.1:n.438+49A>T
NM_153758.3:c.552+49A>T NP_715639.1:n.552+49A>T
NM_001393490.1:c.438+49A>T NP_001380419.1:n.438+49A>T
NM_001393491.1:c.438+49A>T NP_001380420.1:n.438+49A>T
NM_013371.5:c.438+49A>T NP_037503.2:n.438+49A>T
NM_153758.5:c.438+49A>T MANE Select NP_715639.2:n.438+49A>T
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