Canonical Allele Identifier: CA16013870

Gene: IL9R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155999524T>C , CM000685.2:g.155999524T>C	GRCh38
NC_000023.10:g.155229189T>C , CM000685.1:g.155229189T>C	GRCh37
NC_000023.9:g.154882383T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244174.11:c.28+1737T>C MANE Select	ENSP00000244174.5:n.28+1737T>C
ENST00000244174.10:c.28+1737T>C	ENSP00000244174.5:n.28+1737T>C
ENST00000369423.7:c.44+1737T>C	ENSP00000358431.2:n.44+1737T>C
ENST00000489233.6:n.54+1737T>C
XM_011531151.1:c.44+1737T>C	XP_011529453.1:n.44+1737T>C
XM_011531152.1:c.44+1737T>C	XP_011529454.1:n.44+1737T>C
XM_011531153.1:c.28+1737T>C	XP_011529455.1:n.28+1737T>C
XM_011531154.1:c.-215+1737T>C	XP_011529456.1:n.-215+1737T>C
XM_011531155.1:c.44+1737T>C	XP_011529457.1:n.44+1737T>C
XM_011531156.1:c.44+1737T>C	XP_011529458.1:n.44+1737T>C
XM_011531157.1:c.44+1737T>C	XP_011529459.1:n.44+1737T>C
XM_011531151.2:c.44+1737T>C	XP_011529453.1:n.44+1737T>C
XM_011531152.2:c.44+1737T>C	XP_011529454.1:n.44+1737T>C
XM_011531154.2:c.-215+1737T>C	XP_011529456.1:n.-215+1737T>C
XM_011531155.2:c.44+1737T>C	XP_011529457.1:n.44+1737T>C
XM_011531156.2:c.44+1737T>C	XP_011529458.1:n.44+1737T>C
XM_011531157.2:c.44+1737T>C	XP_011529459.1:n.44+1737T>C
XM_017029495.1:c.44+1737T>C	XP_016884984.1:n.44+1737T>C
XM_017029496.1:c.44+1737T>C	XP_016884985.1:n.44+1737T>C
XM_017029497.1:c.-239+1737T>C	XP_016884986.1:n.-239+1737T>C
XM_017029498.1:c.-239+810T>C	XP_016884987.1:n.-239+810T>C
XM_017029499.1:c.-161+810T>C	XP_016884988.1:n.-161+810T>C
XM_017029500.1:c.44+1737T>C	XP_016884989.1:n.44+1737T>C
XM_017029501.1:c.44+1737T>C	XP_016884990.1:n.44+1737T>C
XM_017029502.1:c.28+1737T>C	XP_016884991.1:n.28+1737T>C
XM_017029503.1:c.-137+810T>C	XP_016884992.1:n.-137+810T>C
XM_017029504.1:c.44+1737T>C	XP_016884993.1:n.44+1737T>C
XM_017029505.1:c.44+1737T>C	XP_016884994.1:n.44+1737T>C