Canonical Allele Identifier: CA494707132

Gene: ITGAM

Linked Data

• ClinVar Variation Id: 2066717
• ClinVar RCV Id: RCV002943495
• gnomAD v4: 16-31265410-C-T
• MyVariant Identifiers: chr16:g.31276731C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265410C>T , CM000678.2:g.31265410C>T	GRCh38
NC_000016.9:g.31276731C>T , CM000678.1:g.31276731C>T	GRCh37
NC_000016.8:g.31184232C>T	NCBI36
NG_011719.1:g.10444C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.150C>T MANE Select	ENSP00000441691.3:p.Ala50=
ENST00000648685.1:c.150C>T	ENSP00000496959.1:p.Ala50=
ENST00000287497.12:c.150C>T	ENSP00000287497.8:p.Ala50=
ENST00000544665.7:c.150C>T	ENSP00000441691.2:p.Ala50=
NM_000632.3:c.150C>T	NP_000623.2:p.Ala50=
NM_001145808.1:c.150C>T	NP_001139280.1:p.Ala50=
XM_006721045.1:c.150C>T	XP_006721108.1:p.Ala50=
XM_011545850.1:c.-66C>T	XP_011544152.1:n.-66C>T
XM_011545851.1:c.150C>T	XP_011544153.1:p.Ala50=
XR_950796.1:n.240C>T
XM_011545850.2:c.-66C>T	XP_011544152.1:n.-66C>T
XM_011545851.2:c.150C>T	XP_011544153.1:p.Ala50=
XM_017023216.1:c.150C>T	XP_016878705.1:p.Ala50=
NM_000632.4:c.150C>T MANE Select	NP_000623.2:p.Ala50=
NM_001145808.2:c.150C>T	NP_001139280.1:p.Ala50=