Canonical Allele Identifier: CA12087362
Gene: IL13 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.132658770C>G
GRCh37 chr5:g.131994462C>G
gnomAD v2:
5:131994462 C / G
gnomAD v3:
5:132658770 C / G
gnomAD v4:
chr5-132658770-C-G
Joint Max Group AF 0.93601488 (NFE)
Genomes Max Group AF 0.93620379 (NFE)
Exomes Max Group AF 0.92659313 (NFE)
dbSNP:
1295687
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132658770C>G , CM000667.2:g.132658770C>G GRCh38
NC_000005.9:g.131994462C>G , CM000667.1:g.131994462C>G GRCh37
NC_000005.8:g.132022361C>G NCBI36
NG_012090.1:g.5598C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000304506.7:c.174+410C>G MANE Select ENSP00000304915.3:n.174+410C>G
ENST00000459878.5:n.178+410C>G
ENST00000462480.1:n.598C>G
ENST00000468334.5:n.548-648C>G
ENST00000487267.5:n.345+410C>G
ENST00000617259.2:c.132+410C>G ENSP00000479835.1:n.132+410C>G
NM_002188.2:c.174+410C>G NP_002179.2:n.174+410C>G
NM_001354991.1:c.-22+410C>G NP_001341920.1:n.-22+410C>G
NM_001354992.1:c.-22+410C>G NP_001341921.1:n.-22+410C>G
NM_001354993.1:c.-21-648C>G NP_001341922.1:n.-21-648C>G
NM_002188.3:c.174+410C>G MANE Select NP_002179.2:n.174+410C>G
NM_001354991.2:c.-22+410C>G NP_001341920.1:n.-22+410C>G
NM_001354992.2:c.-22+410C>G NP_001341921.1:n.-22+410C>G
NM_001354993.2:c.-21-648C>G NP_001341922.1:n.-21-648C>G
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