Canonical Allele Identifier: CA2632850839
Gene: ITGAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31265499dup , CM000678.2:g.31265499dup GRCh38
NC_000016.9:g.31276820dup , CM000678.1:g.31276820dup GRCh37
NC_000016.8:g.31184321dup NCBI36
NG_011719.1:g.10533dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000544665.9:c.238+1dup
ENST00000648685.1:c.238+1dup
ENST00000287497.12:c.238+1dup
ENST00000544665.7:c.238+1dup
NM_000632.3:c.238+1dup
NM_001145808.1:c.238+1dup
XM_006721045.1:c.238+1dup
XM_011545850.1:c.23+1dup
XM_011545851.1:c.238+1dup
XR_950796.1:n.328+1dup
XM_011545850.2:c.23+1dup
XM_011545851.2:c.238+1dup
XM_017023216.1:c.238+1dup
NM_000632.4:c.238+1dup
NM_001145808.2:c.238+1dup