Canonical Allele Identifier: CA395682506

Gene: ITGAM

Linked Data

• dbSNP Id: rs771140735
• gnomAD v2: 16-31276730-C-T
• gnomAD v4: 16-31265409-C-T
• MyVariant Identifiers: chr16:g.31276730C>T (hg19) ; chr16:g.31265409C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265409C>T , CM000678.2:g.31265409C>T	GRCh38
NC_000016.9:g.31276730C>T , CM000678.1:g.31276730C>T	GRCh37
NC_000016.8:g.31184231C>T	NCBI36
NG_011719.1:g.10443C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.149C>T MANE Select	ENSP00000441691.3:p.Ala50Val
ENST00000648685.1:c.149C>T	ENSP00000496959.1:p.Ala50Val
ENST00000287497.12:c.149C>T	ENSP00000287497.8:p.Ala50Val
ENST00000544665.7:c.149C>T	ENSP00000441691.2:p.Ala50Val
NM_000632.3:c.149C>T	NP_000623.2:p.Ala50Val
NM_001145808.1:c.149C>T	NP_001139280.1:p.Ala50Val
XM_006721045.1:c.149C>T	XP_006721108.1:p.Ala50Val
XM_011545850.1:c.-67C>T	XP_011544152.1:n.-67C>T
XM_011545851.1:c.149C>T	XP_011544153.1:p.Ala50Val
XR_950796.1:n.239C>T
XM_011545850.2:c.-67C>T	XP_011544152.1:n.-67C>T
XM_011545851.2:c.149C>T	XP_011544153.1:p.Ala50Val
XM_017023216.1:c.149C>T	XP_016878705.1:p.Ala50Val
NM_000632.4:c.149C>T MANE Select	NP_000623.2:p.Ala50Val
NM_001145808.2:c.149C>T	NP_001139280.1:p.Ala50Val