Canonical Allele Identifier: CA8602451
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs777359947
ExAC: 17:42449741 CTCT / C
MyVariant Identifiers: chr17:g.42449742_42449744del (hg19) chr17:g.44372374_44372376del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372376_44372378del , CM000679.2:g.44372376_44372378del GRCh38
NC_000017.10:g.42449744_42449746del , CM000679.1:g.42449744_42449746del GRCh37
NC_000017.9:g.39805270_39805272del NCBI36
NG_008331.1:g.22130_22132del , LRG_479:g.22130_22132del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3108_3110del MANE Select ENSP00000262407.5:p.Glu1037del
ENST00000648408.1:c.2422_2424del
ENST00000262407.5:c.3108_3110del ENSP00000262407.5:p.Glu1037del
ENST00000587295.5:c.301_303del
ENST00000588098.1:c.85_87del
NM_000419.3:c.3108_3110del , LRG_479t1:c.3108_3110del NP_000410.2:p.Glu1037del
XM_011524749.1:c.3006_3008del XP_011523051.1:p.Glu1003del
XM_011524750.1:c.2991_2993del XP_011523052.1:p.Glu998del
NM_000419.4:c.3108_3110del NP_000410.2:p.Glu1037del
NM_000419.5:c.3108_3110del MANE Select NP_000410.2:p.Glu1037del
Search 100 bp 5'
Search 100 bp 3'