Canonical Allele Identifier: CA399791625
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375012G>C , CM000679.2:g.44375012G>C GRCh38
NC_000017.10:g.42452380G>C , CM000679.1:g.42452380G>C GRCh37
NC_000017.9:g.39807906G>C NCBI36
NG_008331.1:g.19494C>G , LRG_479:g.19494C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2827C>G MANE Select ENSP00000262407.5:p.Pro943Ala
ENST00000648408.1:c.2258C>G
ENST00000262407.5:c.2827C>G ENSP00000262407.5:p.Pro943Ala
ENST00000587295.5:c.253+821C>G
ENST00000592462.5:n.2101C>G
NM_000419.3:c.2827C>G , LRG_479t1:c.2827C>G NP_000410.2:p.Pro943Ala
XM_011524749.1:c.2827C>G XP_011523051.1:p.Pro943Ala
XM_011524750.1:c.2827C>G XP_011523052.1:p.Pro943Ala
NM_000419.4:c.2827C>G NP_000410.2:p.Pro943Ala
NM_000419.5:c.2827C>G MANE Select NP_000410.2:p.Pro943Ala