Canonical Allele Identifier: CA719962728
Gene: ITGAM HGNC NCBI

Linked Data

dbSNP Id: rs1226282920

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31322810C>G , CM000678.2:g.31322810C>G GRCh38
NC_000016.9:g.31334131C>G , CM000678.1:g.31334131C>G GRCh37
NC_000016.8:g.31241632C>G NCBI36
NG_011719.1:g.67844C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000544665.9:c.2002+1183C>G MANE Select ENSP00000441691.3:n.2002+1183C>G
ENST00000648685.1:c.2005+1183C>G ENSP00000496959.1:n.2005+1183C>G
ENST00000287497.12:c.2002+1183C>G ENSP00000287497.8:n.2002+1183C>G
ENST00000544665.7:c.2005+1183C>G ENSP00000441691.2:n.2005+1183C>G
ENST00000567031.1:c.454-1589C>G
NM_000632.3:c.2002+1183C>G NP_000623.2:n.2002+1183C>G
NM_001145808.1:c.2005+1183C>G NP_001139280.1:n.2005+1183C>G
XM_011545850.1:c.1819+1183C>G XP_011544152.1:n.1819+1183C>G
XM_011545851.1:c.1841+1439C>G XP_011544153.1:n.1841+1439C>G
XR_950796.1:n.2095+1183C>G
XM_011545850.2:c.1819+1183C>G XP_011544152.1:n.1819+1183C>G
XM_011545851.2:c.1841+1439C>G XP_011544153.1:n.1841+1439C>G
XM_017023216.1:c.2005+1183C>G XP_016878705.1:n.2005+1183C>G
NM_000632.4:c.2002+1183C>G MANE Select NP_000623.2:n.2002+1183C>G
NM_001145808.2:c.2005+1183C>G NP_001139280.1:n.2005+1183C>G