Canonical Allele Identifier: CA2261365712
Gene: ITGA2B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375328A= , CM000679.2:g.44375328A= GRCh38
NC_000017.10:g.42452696A= , CM000679.1:g.42452696A= GRCh37
NC_000017.9:g.39808222A= NCBI36
NG_008331.1:g.19178T= , LRG_479:g.19178T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2728-217T= MANE Select ENSP00000262407.5:n.2728-217T=
ENST00000648408.1:c.2159-217T=
ENST00000262407.5:c.2728-217T= ENSP00000262407.5:n.2728-217T=
ENST00000587295.5:c.253+505T=
ENST00000592462.5:n.1785T=
NM_000419.3:c.2728-217T= , LRG_479t1:c.2728-217T= NP_000410.2:n.2728-217T=
XM_011524749.1:c.2728-217T= XP_011523051.1:n.2728-217T=
XM_011524750.1:c.2728-217T= XP_011523052.1:n.2728-217T=
NM_000419.4:c.2728-217T= NP_000410.2:n.2728-217T=
NM_000419.5:c.2728-217T= MANE Select NP_000410.2:n.2728-217T=
Search 100 bp 5'
Search 100 bp 3'