Canonical Allele Identifier: CA804011323

Gene: IL13

Linked Data

• dbSNP Id: rs1186251418
• MyVariant Identifiers: chr5:g.131993242A>G (hg19) ; chr5:g.132657550A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657550A>G , CM000667.2:g.132657550A>G	GRCh38
NC_000005.9:g.131993242A>G , CM000667.1:g.131993242A>G	GRCh37
NC_000005.8:g.132021141A>G	NCBI36
NG_012090.1:g.4378A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000459878.5:n.108-740A>G
ENST00000468334.5:n.547+306A>G
ENST00000487267.5:n.274+306A>G
NM_001354991.1:c.-92-740A>G	NP_001341920.1:n.-92-740A>G
NM_001354992.1:c.-93+306A>G	NP_001341921.1:n.-93+306A>G
NM_001354993.1:c.-22+306A>G	NP_001341922.1:n.-22+306A>G
NM_001354991.2:c.-92-740A>G	NP_001341920.1:n.-92-740A>G
NM_001354992.2:c.-93+306A>G	NP_001341921.1:n.-93+306A>G
NM_001354993.2:c.-22+306A>G	NP_001341922.1:n.-22+306A>G