Canonical Allele Identifier: CA280603766
Gene: ITGAM HGNC NCBI

Linked Data

dbSNP Id: rs9888739

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31301932C>T , CM000678.2:g.31301932C>T GRCh38
NC_000016.9:g.31313253C>T , CM000678.1:g.31313253C>T GRCh37
NC_000016.8:g.31220754C>T NCBI36
NG_011719.1:g.46966C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000544665.9:c.1707+3978C>T MANE Select ENSP00000441691.3:n.1707+3978C>T
ENST00000648685.1:c.1710+3978C>T ENSP00000496959.1:n.1710+3978C>T
ENST00000287497.12:c.1707+3978C>T ENSP00000287497.8:n.1707+3978C>T
ENST00000544665.7:c.1710+3978C>T ENSP00000441691.2:n.1710+3978C>T
ENST00000567031.1:c.453+4278C>T
NM_000632.3:c.1707+3978C>T NP_000623.2:n.1707+3978C>T
NM_001145808.1:c.1710+3978C>T NP_001139280.1:n.1710+3978C>T
XM_006721045.1:c.1707+3978C>T XP_006721108.1:n.1707+3978C>T
XM_011545850.1:c.1524+3978C>T XP_011544152.1:n.1524+3978C>T
XM_011545851.1:c.1710+3978C>T XP_011544153.1:n.1710+3978C>T
XR_950796.1:n.1800+3978C>T
XM_011545850.2:c.1524+3978C>T XP_011544152.1:n.1524+3978C>T
XM_011545851.2:c.1710+3978C>T XP_011544153.1:n.1710+3978C>T
XM_017023216.1:c.1710+3978C>T XP_016878705.1:n.1710+3978C>T
NM_000632.4:c.1707+3978C>T MANE Select NP_000623.2:n.1707+3978C>T
NM_001145808.2:c.1710+3978C>T NP_001139280.1:n.1710+3978C>T