Canonical Allele Identifier: CA14245452
Gene: ITGAM HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11150610

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31322915C>A , CM000678.2:g.31322915C>A GRCh38
NC_000016.8:g.31241737C>A NCBI36
NC_000016.9:g.31334236C>A , CM000678.1:g.31334236C>A GRCh37
NG_011719.1:g.67949C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287497.12:c.2002+1288C>A ENSP00000287497.8:p.=
ENST00000544665.7:c.2005+1288C>A ENSP00000441691.2:p.=
ENST00000567031.1:n.454-1484C>A
NM_000632.3:c.2002+1288C>A VV NP_000623.2:p.=
NM_001145808.1:c.2005+1288C>A VV NP_001139280.1:p.=
XM_011545850.1:c.1819+1288C>A XP_011544152.1:p.=
XM_011545851.1:c.1842-1484C>A XP_011544153.1:p.=
XR_950796.1:n.2095+1288C>A