Canonical Allele Identifier: CA976367498

Gene: ITGAM

Linked Data

• dbSNP Id: rs2080463041
• gnomAD v3: 16-31322752-T-A
• gnomAD v4: 16-31322752-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31322752T>A , CM000678.2:g.31322752T>A	GRCh38
NC_000016.9:g.31334073T>A , CM000678.1:g.31334073T>A	GRCh37
NC_000016.8:g.31241574T>A	NCBI36
NG_011719.1:g.67786T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000544665.9:c.2002+1125T>A MANE Select	ENSP00000441691.3:n.2002+1125T>A
ENST00000648685.1:c.2005+1125T>A	ENSP00000496959.1:n.2005+1125T>A
ENST00000287497.12:c.2002+1125T>A	ENSP00000287497.8:n.2002+1125T>A
ENST00000544665.7:c.2005+1125T>A	ENSP00000441691.2:n.2005+1125T>A
ENST00000567031.1:c.454-1647T>A
NM_000632.3:c.2002+1125T>A	NP_000623.2:n.2002+1125T>A
NM_001145808.1:c.2005+1125T>A	NP_001139280.1:n.2005+1125T>A
XM_011545850.1:c.1819+1125T>A	XP_011544152.1:n.1819+1125T>A
XM_011545851.1:c.1841+1381T>A	XP_011544153.1:n.1841+1381T>A
XR_950796.1:n.2095+1125T>A
XM_011545850.2:c.1819+1125T>A	XP_011544152.1:n.1819+1125T>A
XM_011545851.2:c.1841+1381T>A	XP_011544153.1:n.1841+1381T>A
XM_017023216.1:c.2005+1125T>A	XP_016878705.1:n.2005+1125T>A
NM_000632.4:c.2002+1125T>A MANE Select	NP_000623.2:n.2002+1125T>A
NM_001145808.2:c.2005+1125T>A	NP_001139280.1:n.2005+1125T>A