Canonical Allele Identifier: CA399787793
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372393G>T , CM000679.2:g.44372393G>T GRCh38
NC_000017.10:g.42449761G>T , CM000679.1:g.42449761G>T GRCh37
NC_000017.9:g.39805287G>T NCBI36
NG_008331.1:g.22113C>A , LRG_479:g.22113C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3091C>A MANE Select ENSP00000262407.5:p.Leu1031Met
ENST00000648408.1:c.2405C>A
ENST00000262407.5:c.3091C>A ENSP00000262407.5:p.Leu1031Met
ENST00000587295.5:c.284C>A
ENST00000588098.1:c.68C>A
NM_000419.3:c.3091C>A , LRG_479t1:c.3091C>A NP_000410.2:p.Leu1031Met
XM_011524749.1:c.2989C>A XP_011523051.1:p.Leu997Met
XM_011524750.1:c.2974C>A XP_011523052.1:p.Leu992Met
NM_000419.4:c.3091C>A NP_000410.2:p.Leu1031Met
NM_000419.5:c.3091C>A MANE Select NP_000410.2:p.Leu1031Met