Canonical Allele Identifier: CA494707091

Gene: ITGAM

Linked Data

• MyVariant Identifiers: chr16:g.31276722G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265401G>C , CM000678.2:g.31265401G>C	GRCh38
NC_000016.9:g.31276722G>C , CM000678.1:g.31276722G>C	GRCh37
NC_000016.8:g.31184223G>C	NCBI36
NG_011719.1:g.10435G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000544665.9:c.141G>C MANE Select	ENSP00000441691.3:p.Val47=
ENST00000648685.1:c.141G>C	ENSP00000496959.1:p.Val47=
ENST00000287497.12:c.141G>C	ENSP00000287497.8:p.Val47=
ENST00000544665.7:c.141G>C	ENSP00000441691.2:p.Val47=
NM_000632.3:c.141G>C	NP_000623.2:p.Val47=
NM_001145808.1:c.141G>C	NP_001139280.1:p.Val47=
XM_006721045.1:c.141G>C	XP_006721108.1:p.Val47=
XM_011545850.1:c.-75G>C	XP_011544152.1:n.-75G>C
XM_011545851.1:c.141G>C	XP_011544153.1:p.Val47=
XR_950796.1:n.231G>C
XM_011545850.2:c.-75G>C	XP_011544152.1:n.-75G>C
XM_011545851.2:c.141G>C	XP_011544153.1:p.Val47=
XM_017023216.1:c.141G>C	XP_016878705.1:p.Val47=
NM_000632.4:c.141G>C MANE Select	NP_000623.2:p.Val47=
NM_001145808.2:c.141G>C	NP_001139280.1:p.Val47=