Canonical Allele Identifier: CA1358123013
Gene: ITGA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562558A= , CM000665.2:g.37562558A= GRCh38
NC_000003.11:g.37604049A= , CM000665.1:g.37604049A= GRCh37
NC_000003.10:g.37579053A= NCBI36
NG_016166.1:g.115237A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19973A= MANE Select ENSP00000264741.5:n.1689+19973A=
ENST00000264741.9:c.1689+19973A= ENSP00000264741.5:n.1689+19973A=
ENST00000422441.5:c.1689+19973A= ENSP00000397258.1:n.1689+19973A=
NM_002207.2:c.1689+19973A= NP_002198.2:n.1689+19973A=
NM_002207.3:c.1689+19973A= MANE Select NP_002198.2:n.1689+19973A=