Canonical Allele Identifier: CA1358123012
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs1699504030

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562557C>T , CM000665.2:g.37562557C>T GRCh38
NC_000003.11:g.37604048C>T , CM000665.1:g.37604048C>T GRCh37
NC_000003.10:g.37579052C>T NCBI36
NG_016166.1:g.115236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19972C>T MANE Select ENSP00000264741.5:n.1689+19972C>T
ENST00000264741.9:c.1689+19972C>T ENSP00000264741.5:n.1689+19972C>T
ENST00000422441.5:c.1689+19972C>T ENSP00000397258.1:n.1689+19972C>T
NM_002207.2:c.1689+19972C>T NP_002198.2:n.1689+19972C>T
NM_002207.3:c.1689+19972C>T MANE Select NP_002198.2:n.1689+19972C>T