Canonical Allele Identifier: CA280615633
Gene: ITGAM HGNC NCBI

Linked Data

dbSNP Id: rs191073117

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31322802C>T , CM000678.2:g.31322802C>T GRCh38
NC_000016.9:g.31334123C>T , CM000678.1:g.31334123C>T GRCh37
NC_000016.8:g.31241624C>T NCBI36
NG_011719.1:g.67836C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000544665.9:c.2002+1175C>T MANE Select ENSP00000441691.3:n.2002+1175C>T
ENST00000648685.1:c.2005+1175C>T ENSP00000496959.1:n.2005+1175C>T
ENST00000287497.12:c.2002+1175C>T ENSP00000287497.8:n.2002+1175C>T
ENST00000544665.7:c.2005+1175C>T ENSP00000441691.2:n.2005+1175C>T
ENST00000567031.1:c.454-1597C>T
NM_000632.3:c.2002+1175C>T NP_000623.2:n.2002+1175C>T
NM_001145808.1:c.2005+1175C>T NP_001139280.1:n.2005+1175C>T
XM_011545850.1:c.1819+1175C>T XP_011544152.1:n.1819+1175C>T
XM_011545851.1:c.1841+1431C>T XP_011544153.1:n.1841+1431C>T
XR_950796.1:n.2095+1175C>T
XM_011545850.2:c.1819+1175C>T XP_011544152.1:n.1819+1175C>T
XM_011545851.2:c.1841+1431C>T XP_011544153.1:n.1841+1431C>T
XM_017023216.1:c.2005+1175C>T XP_016878705.1:n.2005+1175C>T
NM_000632.4:c.2002+1175C>T MANE Select NP_000623.2:n.2002+1175C>T
NM_001145808.2:c.2005+1175C>T NP_001139280.1:n.2005+1175C>T