Canonical Allele Identifier: CA2739546777
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44380809C>A , CM000679.2:g.44380809C>A GRCh38
NC_000017.10:g.42458177C>A , CM000679.1:g.42458177C>A GRCh37
NC_000017.9:g.39813703C>A NCBI36
NG_008331.1:g.13697G>T , LRG_479:g.13697G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1393+70G>T MANE Select ENSP00000262407.5:n.1393+70G>T
ENST00000648408.1:c.824+70G>T
ENST00000262407.5:c.1393+70G>T ENSP00000262407.5:n.1393+70G>T
ENST00000592226.5:n.703G>T
ENST00000592462.5:n.188+70G>T
NM_000419.3:c.1393+70G>T , LRG_479t1:c.1393+70G>T NP_000410.2:n.1393+70G>T
XM_011524749.1:c.1393+70G>T XP_011523051.1:n.1393+70G>T
XM_011524750.1:c.1393+70G>T XP_011523052.1:n.1393+70G>T
NM_000419.4:c.1393+70G>T NP_000410.2:n.1393+70G>T
NM_000419.5:c.1393+70G>T MANE Select NP_000410.2:n.1393+70G>T