Canonical Allele Identifier: CA2261365705
Gene: ITGA2B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375320C= , CM000679.2:g.44375320C= GRCh38
NC_000017.10:g.42452688C= , CM000679.1:g.42452688C= GRCh37
NC_000017.9:g.39808214C= NCBI36
NG_008331.1:g.19186G= , LRG_479:g.19186G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2728-209G= MANE Select ENSP00000262407.5:n.2728-209G=
ENST00000648408.1:c.2159-209G=
ENST00000262407.5:c.2728-209G= ENSP00000262407.5:n.2728-209G=
ENST00000587295.5:c.253+513G=
ENST00000592462.5:n.1793G=
NM_000419.3:c.2728-209G= , LRG_479t1:c.2728-209G= NP_000410.2:n.2728-209G=
XM_011524749.1:c.2728-209G= XP_011523051.1:n.2728-209G=
XM_011524750.1:c.2728-209G= XP_011523052.1:n.2728-209G=
NM_000419.4:c.2728-209G= NP_000410.2:n.2728-209G=
NM_000419.5:c.2728-209G= MANE Select NP_000410.2:n.2728-209G=
Search 100 bp 5'
Search 100 bp 3'