Canonical Allele Identifier: CA410482447
Gene: ITGB2 HGNC NCBI

Linked Data

dbSNP Id: rs1601277528

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44886786G>A , CM000683.2:g.44886786G>A GRCh38
NC_000021.8:g.46306701G>A , CM000683.1:g.46306701G>A GRCh37
NC_000021.7:g.45131129G>A NCBI36
NG_007270.2:g.47053C>T , LRG_76:g.47053C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696946.1:n.1404C>T
ENST00000302347.10:c.2269C>T ENSP00000303242.6:p.Arg757Trp
ENST00000652462.1:c.2197C>T MANE Select ENSP00000498780.1:p.Arg733Trp
ENST00000302347.9:c.2197C>T ENSP00000303242.5:p.Arg733Trp
ENST00000355153.8:c.2197C>T ENSP00000347279.4:p.Arg733Trp
ENST00000397850.6:c.2197C>T ENSP00000380948.2:p.Arg733Trp
ENST00000397852.5:c.2197C>T ENSP00000380950.1:p.Arg733Trp
ENST00000397854.7:c.2026C>T ENSP00000380952.3:p.Arg676Trp
ENST00000397857.5:c.2197C>T ENSP00000380955.1:p.Arg733Trp
ENST00000475170.5:n.1597C>T
ENST00000479202.5:n.556C>T
ENST00000498666.5:n.4253C>T
ENST00000523323.5:c.*2024C>T ENSP00000427732.1:n.*2024C>T
ENST00000610622.4:c.*888C>T ENSP00000480700.1:n.*888C>T
NM_000211.4:c.2197C>T NP_000202.3:p.Arg733Trp
NM_001127491.2:c.2197C>T NP_001120963.2:p.Arg733Trp
NM_001303238.1:c.1990C>T NP_001290167.1:p.Arg664Trp
XM_006724001.1:c.1990C>T XP_006724064.1:p.Arg664Trp
XM_006724001.2:c.1990C>T XP_006724064.1:p.Arg664Trp
NM_000211.5:c.2197C>T MANE Select NP_000202.3:p.Arg733Trp
NM_001127491.3:c.2197C>T NP_001120963.2:p.Arg733Trp
NM_001303238.2:c.1990C>T NP_001290167.1:p.Arg664Trp