Canonical Allele Identifier: CA360944377

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995965G>C (hg19) ; chr5:g.132660273G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660273G>C , CM000667.2:g.132660273G>C	GRCh38
NC_000005.9:g.131995965G>C , CM000667.1:g.131995965G>C	GRCh37
NC_000005.8:g.132023864G>C	NCBI36
NG_012090.1:g.7101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.432G>C MANE Select	ENSP00000304915.3:p.Gln144His
ENST00000459878.5:n.436G>C
ENST00000462480.1:n.1503G>C
ENST00000468334.5:n.805G>C
ENST00000487267.5:n.603G>C
ENST00000617259.2:c.390G>C	ENSP00000479835.1:p.Gln130His
NM_002188.2:c.432G>C	NP_002179.2:p.Gln144His
NM_001354991.1:c.237G>C	NP_001341920.1:p.Gln79His
NM_001354992.1:c.237G>C	NP_001341921.1:p.Gln79His
NM_001354993.1:c.237G>C	NP_001341922.1:p.Gln79His
NM_002188.3:c.432G>C MANE Select	NP_002179.2:p.Gln144His
NM_001354991.2:c.237G>C	NP_001341920.1:p.Gln79His
NM_001354992.2:c.237G>C	NP_001341921.1:p.Gln79His
NM_001354993.2:c.237G>C	NP_001341922.1:p.Gln79His