Canonical Allele Identifier: CA127251606

Gene: IL13

Linked Data

• dbSNP Id: rs56258826
• MyVariant Identifiers: chr5:g.131995970A>C (hg19) ; chr5:g.132660278A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660278A>C , CM000667.2:g.132660278A>C	GRCh38
NC_000005.9:g.131995970A>C , CM000667.1:g.131995970A>C	GRCh37
NC_000005.8:g.132023869A>C	NCBI36
NG_012090.1:g.7106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.437A>C MANE Select	ENSP00000304915.3:p.Asn146Thr
ENST00000459878.5:n.441A>C
ENST00000462480.1:n.1508A>C
ENST00000468334.5:n.810A>C
ENST00000487267.5:n.608A>C
ENST00000617259.2:c.395A>C	ENSP00000479835.1:p.Asn132Thr
NM_002188.2:c.437A>C	NP_002179.2:p.Asn146Thr
NM_001354991.1:c.242A>C	NP_001341920.1:p.Asn81Thr
NM_001354992.1:c.242A>C	NP_001341921.1:p.Asn81Thr
NM_001354993.1:c.242A>C	NP_001341922.1:p.Asn81Thr
NM_002188.3:c.437A>C MANE Select	NP_002179.2:p.Asn146Thr
NM_001354991.2:c.242A>C	NP_001341920.1:p.Asn81Thr
NM_001354992.2:c.242A>C	NP_001341921.1:p.Asn81Thr
NM_001354993.2:c.242A>C	NP_001341922.1:p.Asn81Thr