Canonical Allele Identifier: CA127249199

Gene: IL13

Linked Data

• dbSNP Id: rs560993434
• gnomAD v2: 5-131993190-CA-C
• gnomAD v3: 5-132657498-CA-C
• gnomAD v4: 5-132657498-CA-C
• MyVariant Identifiers: chr5:g.131993191del (hg19) ; chr5:g.132657499del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657502del , CM000667.2:g.132657502del	GRCh38
NC_000005.9:g.131993194del , CM000667.1:g.131993194del	GRCh37
NC_000005.8:g.132021093del	NCBI36
NG_012090.1:g.4330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000459878.5:n.108-788del
ENST00000468334.5:n.547+258del
ENST00000487267.5:n.274+258del
NM_001354991.1:c.-92-788del	NP_001341920.1:n.-92-788del
NM_001354992.1:c.-93+258del	NP_001341921.1:n.-93+258del
NM_001354993.1:c.-22+258del	NP_001341922.1:n.-22+258del
NM_001354991.2:c.-92-788del	NP_001341920.1:n.-92-788del
NM_001354992.2:c.-93+258del	NP_001341921.1:n.-93+258del
NM_001354993.2:c.-22+258del	NP_001341922.1:n.-22+258del