Canonical Allele Identifier: CA984231874
Gene: ITGB3 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47300211G>A , CM000679.2:g.47300211G>A GRCh38
NC_000017.10:g.45377577G>A , CM000679.1:g.45377577G>A GRCh37
NC_000017.9:g.42732576G>A NCBI36
NG_008332.2:g.51370G>A , LRG_481:g.51370G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.1914-267G>A ENSP00000513002.1:n.1914-267G>A
ENST00000559488.7:c.1914-267G>A MANE Select ENSP00000452786.2:n.1914-267G>A
ENST00000559488.5:c.1914-267G>A ENSP00000452786.1:n.1914-267G>A
ENST00000560629.1:c.1879-267G>A
NM_000212.2:c.1914-267G>A , LRG_481t1:c.1914-267G>A NP_000203.2:n.1914-267G>A
NM_000212.3:c.1914-267G>A MANE Select NP_000203.2:n.1914-267G>A