Canonical Allele Identifier: CA494719398

Gene: ITGAM

Linked Data

• MyVariant Identifiers: chr16:g.31334113C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31322792C>G , CM000678.2:g.31322792C>G	GRCh38
NC_000016.9:g.31334113C>G , CM000678.1:g.31334113C>G	GRCh37
NC_000016.8:g.31241614C>G	NCBI36
NG_011719.1:g.67826C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.2002+1165C>G MANE Select	ENSP00000441691.3:n.2002+1165C>G
ENST00000648685.1:c.2005+1165C>G	ENSP00000496959.1:n.2005+1165C>G
ENST00000287497.12:c.2002+1165C>G	ENSP00000287497.8:n.2002+1165C>G
ENST00000544665.7:c.2005+1165C>G	ENSP00000441691.2:n.2005+1165C>G
ENST00000567031.1:c.454-1607C>G
NM_000632.3:c.2002+1165C>G	NP_000623.2:n.2002+1165C>G
NM_001145808.1:c.2005+1165C>G	NP_001139280.1:n.2005+1165C>G
XM_011545850.1:c.1819+1165C>G	XP_011544152.1:n.1819+1165C>G
XM_011545851.1:c.1841+1421C>G	XP_011544153.1:n.1841+1421C>G
XR_950796.1:n.2095+1165C>G
XM_011545850.2:c.1819+1165C>G	XP_011544152.1:n.1819+1165C>G
XM_011545851.2:c.1841+1421C>G	XP_011544153.1:n.1841+1421C>G
XM_017023216.1:c.2005+1165C>G	XP_016878705.1:n.2005+1165C>G
NM_000632.4:c.2002+1165C>G MANE Select	NP_000623.2:n.2002+1165C>G
NM_001145808.2:c.2005+1165C>G	NP_001139280.1:n.2005+1165C>G