Canonical Allele Identifier: CA2638213176
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44372205-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372205C>G , CM000679.2:g.44372205C>G GRCh38
NC_000017.10:g.42449573C>G , CM000679.1:g.42449573C>G GRCh37
NC_000017.9:g.39805099C>G NCBI36
NG_008331.1:g.22301G>C , LRG_479:g.22301G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*159G>C MANE Select ENSP00000262407.5:n.*159G>C
ENST00000648408.1:c.2593G>C
ENST00000262407.5:c.*159G>C ENSP00000262407.5:n.*159G>C
ENST00000587295.5:c.472G>C
ENST00000588098.1:c.256G>C
NM_000419.3:c.*159G>C , LRG_479t1:c.*159G>C NP_000410.2:n.*159G>C
XM_011524749.1:c.*159G>C XP_011523051.1:n.*159G>C
XM_011524750.1:c.*159G>C XP_011523052.1:n.*159G>C
NM_000419.4:c.*159G>C NP_000410.2:n.*159G>C
NM_000419.5:c.*159G>C MANE Select NP_000410.2:n.*159G>C
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