Canonical Allele Identifier: CA562773163

Gene: IL13

Linked Data

• dbSNP Id: rs986414149
• gnomAD v2: 5-131993205-C-CA
• gnomAD v3: 5-132657513-C-CA
• gnomAD v4: 5-132657513-C-CA
• MyVariant Identifiers: chr5:g.131993205_131993206insA (hg19) ; chr5:g.132657513_132657514insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657520dup , CM000667.2:g.132657520dup	GRCh38
NC_000005.9:g.131993212dup , CM000667.1:g.131993212dup	GRCh37
NC_000005.8:g.132021111dup	NCBI36
NG_012090.1:g.4348dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.108-770dup
ENST00000468334.5:n.547+276dup
ENST00000487267.5:n.274+276dup
NM_001354991.1:c.-92-770dup	NP_001341920.1:n.-92-770dup
NM_001354992.1:c.-93+276dup	NP_001341921.1:n.-93+276dup
NM_001354993.1:c.-22+276dup	NP_001341922.1:n.-22+276dup
NM_001354991.2:c.-92-770dup	NP_001341920.1:n.-92-770dup
NM_001354992.2:c.-93+276dup	NP_001341921.1:n.-93+276dup
NM_001354993.2:c.-22+276dup	NP_001341922.1:n.-22+276dup