Canonical Allele Identifier: CA400020489
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283384C>A , CM000679.2:g.47283384C>A GRCh38
NC_000017.10:g.45360750C>A , CM000679.1:g.45360750C>A GRCh37
NC_000017.9:g.42715749C>A NCBI36
NG_008332.2:g.34543C>A , LRG_481:g.34543C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.196C>A ENSP00000513002.1:p.Leu66Met
ENST00000559488.7:c.196C>A MANE Select ENSP00000452786.2:p.Leu66Met
ENST00000559488.5:c.196C>A ENSP00000452786.1:p.Leu66Met
ENST00000560629.1:c.161C>A
ENST00000571680.1:c.196C>A ENSP00000461626.1:p.Leu66Met
NM_000212.2:c.196C>A , LRG_481t1:c.196C>A NP_000203.2:p.Leu66Met
NM_000212.3:c.196C>A MANE Select NP_000203.2:p.Leu66Met