Canonical Allele Identifier: CA1358084405
Gene: ITGA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37475999C= , CM000665.2:g.37475999C= GRCh38
NC_000003.11:g.37517490C= , CM000665.1:g.37517490C= GRCh37
NC_000003.10:g.37492494C= NCBI36
NG_016166.1:g.28678C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264741.10:c.420+2539C= MANE Select ENSP00000264741.5:n.420+2539C=
ENST00000264741.9:c.420+2539C= ENSP00000264741.5:n.420+2539C=
ENST00000422441.5:c.420+2539C= ENSP00000397258.1:n.420+2539C=
NM_002207.2:c.420+2539C= NP_002198.2:n.420+2539C=
NM_002207.3:c.420+2539C= MANE Select NP_002198.2:n.420+2539C=
Search 100 bp 5'
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