Canonical Allele Identifier: CA280602647

Gene: ITGAM

Linked Data

• dbSNP Id: rs977892762
• gnomAD v3: 16-31265496-A-AGGGT
• gnomAD v4: 16-31265496-A-AGGGT
• MyVariant Identifiers: chr16:g.31276817_31276818insGGGT (hg19) ; chr16:g.31265496_31265497insGGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265498_31265501dup , CM000678.2:g.31265498_31265501dup	GRCh38
NC_000016.9:g.31276819_31276822dup , CM000678.1:g.31276819_31276822dup	GRCh37
NC_000016.8:g.31184320_31184323dup	NCBI36
NG_011719.1:g.10532_10535dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.238_238+3dup
ENST00000648685.1:c.238_238+3dup
ENST00000287497.12:c.238_238+3dup
ENST00000544665.7:c.238_238+3dup
NM_000632.3:c.238_238+3dup
NM_001145808.1:c.238_238+3dup
XM_006721045.1:c.238_238+3dup
XM_011545850.1:c.23_23+3dup
XM_011545851.1:c.238_238+3dup
XR_950796.1:n.328_328+3dup
XM_011545850.2:c.23_23+3dup
XM_011545851.2:c.238_238+3dup
XM_017023216.1:c.238_238+3dup
NM_000632.4:c.238_238+3dup
NM_001145808.2:c.238_238+3dup