Canonical Allele Identifier: CA1358122944
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs1699502435

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562414A>G , CM000665.2:g.37562414A>G GRCh38
NC_000003.11:g.37603905A>G , CM000665.1:g.37603905A>G GRCh37
NC_000003.10:g.37578909A>G NCBI36
NG_016166.1:g.115093A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19829A>G MANE Select ENSP00000264741.5:n.1689+19829A>G
ENST00000264741.9:c.1689+19829A>G ENSP00000264741.5:n.1689+19829A>G
ENST00000422441.5:c.1689+19829A>G ENSP00000397258.1:n.1689+19829A>G
NM_002207.2:c.1689+19829A>G NP_002198.2:n.1689+19829A>G
NM_002207.3:c.1689+19829A>G MANE Select NP_002198.2:n.1689+19829A>G