Canonical Allele Identifier: CA2261364469
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372639_44372640delinsCT , CM000679.2:g.44372639_44372640delinsCT GRCh38
NC_000017.10:g.42450007_42450008delinsCT , CM000679.1:g.42450007_42450008delinsCT GRCh37
NC_000017.9:g.39805533_39805534delinsCT NCBI36
NG_008331.1:g.21866_21867delinsAG , LRG_479:g.21866_21867delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-217_3061-216delinsAG MANE Select ENSP00000262407.5:n.3061-217_3061-216delinsAG
ENST00000648408.1:c.2375-217_2375-216delinsAG
ENST00000262407.5:c.3061-217_3061-216delinsAG ENSP00000262407.5:n.3061-217_3061-216delinsAG
ENST00000587295.5:c.254-217_254-216delinsAG
ENST00000588098.1:c.38-217_38-216delinsAG
NM_000419.3:c.3061-217_3061-216delinsAG , LRG_479t1:c.3061-217_3061-216delinsAG NP_000410.2:n.3061-217_3061-216delinsAG
XM_011524749.1:c.2959-217_2959-216delinsAG XP_011523051.1:n.2959-217_2959-216delinsAG
XM_011524750.1:c.2944-217_2944-216delinsAG XP_011523052.1:n.2944-217_2944-216delinsAG
NM_000419.4:c.3061-217_3061-216delinsAG NP_000410.2:n.3061-217_3061-216delinsAG
NM_000419.5:c.3061-217_3061-216delinsAG MANE Select NP_000410.2:n.3061-217_3061-216delinsAG
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