Canonical Allele Identifier: CA1358084347
Gene: ITGA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37475876G= , CM000665.2:g.37475876G= GRCh38
NC_000003.11:g.37517367G= , CM000665.1:g.37517367G= GRCh37
NC_000003.10:g.37492371G= NCBI36
NG_016166.1:g.28555G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264741.10:c.420+2416G= MANE Select ENSP00000264741.5:n.420+2416G=
ENST00000264741.9:c.420+2416G= ENSP00000264741.5:n.420+2416G=
ENST00000422441.5:c.420+2416G= ENSP00000397258.1:n.420+2416G=
NM_002207.2:c.420+2416G= NP_002198.2:n.420+2416G=
NM_002207.3:c.420+2416G= MANE Select NP_002198.2:n.420+2416G=
Search 100 bp 5'
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