Canonical Allele Identifier: CA494707411

Gene: ITGAM

Linked Data

• gnomAD v4: 16-31265476-A-G
• MyVariant Identifiers: chr16:g.31276797A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265476A>G , CM000678.2:g.31265476A>G	GRCh38
NC_000016.9:g.31276797A>G , CM000678.1:g.31276797A>G	GRCh37
NC_000016.8:g.31184298A>G	NCBI36
NG_011719.1:g.10510A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.216A>G MANE Select	ENSP00000441691.3:p.Ser72=
ENST00000648685.1:c.216A>G	ENSP00000496959.1:p.Ser72=
ENST00000287497.12:c.216A>G	ENSP00000287497.8:p.Ser72=
ENST00000544665.7:c.216A>G	ENSP00000441691.2:p.Ser72=
NM_000632.3:c.216A>G	NP_000623.2:p.Ser72=
NM_001145808.1:c.216A>G	NP_001139280.1:p.Ser72=
XM_006721045.1:c.216A>G	XP_006721108.1:p.Ser72=
XM_011545850.1:c.1A>G	XP_011544152.1:p.Met1Val
XM_011545851.1:c.216A>G	XP_011544153.1:p.Ser72=
XR_950796.1:n.306A>G
XM_011545850.2:c.1A>G	XP_011544152.1:p.Met1Val
XM_011545851.2:c.216A>G	XP_011544153.1:p.Ser72=
XM_017023216.1:c.216A>G	XP_016878705.1:p.Ser72=
NM_000632.4:c.216A>G MANE Select	NP_000623.2:p.Ser72=
NM_001145808.2:c.216A>G	NP_001139280.1:p.Ser72=