Canonical Allele Identifier: CA1358122959

Gene: ITGA9

Linked Data

• dbSNP Id: rs1699502700

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37562447T>C , CM000665.2:g.37562447T>C	GRCh38
NC_000003.11:g.37603938T>C , CM000665.1:g.37603938T>C	GRCh37
NC_000003.10:g.37578942T>C	NCBI36
NG_016166.1:g.115126T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264741.10:c.1689+19862T>C MANE Select	ENSP00000264741.5:n.1689+19862T>C
ENST00000264741.9:c.1689+19862T>C	ENSP00000264741.5:n.1689+19862T>C
ENST00000422441.5:c.1689+19862T>C	ENSP00000397258.1:n.1689+19862T>C
NM_002207.2:c.1689+19862T>C	NP_002198.2:n.1689+19862T>C
NM_002207.3:c.1689+19862T>C MANE Select	NP_002198.2:n.1689+19862T>C