Canonical Allele Identifier: CA12087361
Gene: IL13 HGNC NCBI

Linked Data

dbSNP Id: rs2066960
gnomAD v2: 5-131994435-C-A
gnomAD v3: 5-132658743-C-A
gnomAD v4: 5-132658743-C-A
MyVariant Identifiers: chr5:g.131994435C>A (hg19) chr5:g.132658743C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132658743C>A , CM000667.2:g.132658743C>A GRCh38
NC_000005.9:g.131994435C>A , CM000667.1:g.131994435C>A GRCh37
NC_000005.8:g.132022334C>A NCBI36
NG_012090.1:g.5571C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000304506.7:c.174+383C>A MANE Select ENSP00000304915.3:n.174+383C>A
ENST00000459878.5:n.178+383C>A
ENST00000462480.1:n.571C>A
ENST00000468334.5:n.548-675C>A
ENST00000487267.5:n.345+383C>A
ENST00000617259.2:c.132+383C>A ENSP00000479835.1:n.132+383C>A
NM_002188.2:c.174+383C>A NP_002179.2:n.174+383C>A
NM_001354991.1:c.-22+383C>A NP_001341920.1:n.-22+383C>A
NM_001354992.1:c.-22+383C>A NP_001341921.1:n.-22+383C>A
NM_001354993.1:c.-21-675C>A NP_001341922.1:n.-21-675C>A
NM_002188.3:c.174+383C>A MANE Select NP_002179.2:n.174+383C>A
NM_001354991.2:c.-22+383C>A NP_001341920.1:n.-22+383C>A
NM_001354992.2:c.-22+383C>A NP_001341921.1:n.-22+383C>A
NM_001354993.2:c.-21-675C>A NP_001341922.1:n.-21-675C>A
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