Canonical Allele Identifier: CA2581496584
Gene: IL9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894824G>T , CM000667.2:g.135894824G>T GRCh38
NC_000005.9:g.135230513G>T , CM000667.1:g.135230513G>T GRCh37
NC_000005.8:g.135258412G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274520.2:c.183+616C>A MANE Select ENSP00000274520.1:n.183+616C>A
ENST00000274520.1:c.183+616C>A ENSP00000274520.1:n.183+616C>A
NM_000590.1:c.183+616C>A NP_000581.1:n.183+616C>A
NM_000590.2:c.183+616C>A MANE Select NP_000581.1:n.183+616C>A