Canonical Allele Identifier: CA804010881

Gene: IL13

Linked Data

• dbSNP Id: rs1261070434
• gnomAD v4: 5-132656959-C-T
• MyVariant Identifiers: chr5:g.131992651C>T (hg19) ; chr5:g.132656959C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132656959C>T , CM000667.2:g.132656959C>T	GRCh38
NC_000005.9:g.131992651C>T , CM000667.1:g.131992651C>T	GRCh37
NC_000005.8:g.132020550C>T	NCBI36
NG_012090.1:g.3787C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.107+329C>T
ENST00000468334.5:n.369-107C>T
ENST00000487267.5:n.96-107C>T
NM_001354991.1:c.-93+329C>T	NP_001341920.1:n.-93+329C>T
NM_001354992.1:c.-271-107C>T	NP_001341921.1:n.-271-107C>T
NM_001354993.1:c.-200-107C>T	NP_001341922.1:n.-200-107C>T
NM_001354991.2:c.-93+329C>T	NP_001341920.1:n.-93+329C>T
NM_001354992.2:c.-271-107C>T	NP_001341921.1:n.-271-107C>T
NM_001354993.2:c.-200-107C>T	NP_001341922.1:n.-200-107C>T