Canonical Allele Identifier: CA500260767
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42449777C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372409C>T , CM000679.2:g.44372409C>T GRCh38
NC_000017.10:g.42449777C>T , CM000679.1:g.42449777C>T GRCh37
NC_000017.9:g.39805303C>T NCBI36
NG_008331.1:g.22097G>A , LRG_479:g.22097G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.3075G>A MANE Select ENSP00000262407.5:p.Lys1025=
ENST00000648408.1:c.2389G>A
ENST00000262407.5:c.3075G>A ENSP00000262407.5:p.Lys1025=
ENST00000587295.5:c.268G>A
ENST00000588098.1:c.52G>A
NM_000419.3:c.3075G>A , LRG_479t1:c.3075G>A NP_000410.2:p.Lys1025=
XM_011524749.1:c.2973G>A XP_011523051.1:p.Lys991=
XM_011524750.1:c.2958G>A XP_011523052.1:p.Lys986=
NM_000419.4:c.3075G>A NP_000410.2:p.Lys1025=
NM_000419.5:c.3075G>A MANE Select NP_000410.2:p.Lys1025=