Canonical Allele Identifier: CA2471509214
Gene: IL9R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.57184462T>C , CM000686.2:g.57184462T>C GRCh38
NC_000024.9:g.59330613T>C , CM000686.1:g.59330613T>C GRCh37
NC_000024.8:g.57740001T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000711286.1:c.28+155T>C ENSP00000518617.1:n.28+155T>C
ENST00000711287.1:c.44+155T>C ENSP00000518616.1:n.44+155T>C
ENST00000711288.1:n.54+155T>C
XM_011545645.1:c.44+155T>C XP_011543947.1:n.44+155T>C
XM_011545646.1:c.44+155T>C XP_011543948.1:n.44+155T>C
XM_011545647.1:c.28+155T>C XP_011543949.1:n.28+155T>C
XM_011545649.1:c.-215+155T>C XP_011543951.1:n.-215+155T>C
XM_011545650.1:c.44+155T>C XP_011543952.1:n.44+155T>C
XM_011545651.1:c.44+155T>C XP_011543953.1:n.44+155T>C
XM_011545652.1:c.44+155T>C XP_011543954.1:n.44+155T>C
XM_011545645.2:c.44+155T>C XP_011543947.1:n.44+155T>C
XM_011545646.2:c.44+155T>C XP_011543948.1:n.44+155T>C
XM_011545649.2:c.-215+155T>C XP_011543951.1:n.-215+155T>C
XM_011545650.2:c.44+155T>C XP_011543952.1:n.44+155T>C
XM_011545651.2:c.44+155T>C XP_011543953.1:n.44+155T>C
XM_011545652.2:c.44+155T>C XP_011543954.1:n.44+155T>C
XM_017030044.1:c.44+155T>C XP_016885533.1:n.44+155T>C
XM_017030045.1:c.44+155T>C XP_016885534.1:n.44+155T>C
XM_017030046.1:c.-239+155T>C XP_016885535.1:n.-239+155T>C
XM_017030047.1:c.-359+155T>C XP_016885536.1:n.-359+155T>C
XM_017030048.1:c.-281+155T>C XP_016885537.1:n.-281+155T>C
XM_017030049.1:c.44+155T>C XP_016885538.1:n.44+155T>C
XM_017030050.1:c.44+155T>C XP_016885539.1:n.44+155T>C
XM_017030051.1:c.28+155T>C XP_016885540.1:n.28+155T>C
XM_017030052.1:c.-257+155T>C XP_016885541.1:n.-257+155T>C
XM_017030053.1:c.44+155T>C XP_016885542.1:n.44+155T>C
XM_017030054.1:c.44+155T>C XP_016885543.1:n.44+155T>C