Canonical Allele Identifier: CA2576290851
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374271A>C , CM000679.2:g.44374271A>C GRCh38
NC_000017.10:g.42451639A>C , CM000679.1:g.42451639A>C GRCh37
NC_000017.9:g.39807165A>C NCBI36
NG_008331.1:g.20235T>G , LRG_479:g.20235T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.3060+83T>G MANE Select ENSP00000262407.5:n.3060+83T>G
ENST00000648408.1:c.2374+388T>G
ENST00000262407.5:c.3060+83T>G ENSP00000262407.5:n.3060+83T>G
ENST00000587295.5:c.253+1562T>G
ENST00000588098.1:c.37+388T>G
ENST00000592462.5:n.2842T>G
NM_000419.3:c.3060+83T>G , LRG_479t1:c.3060+83T>G NP_000410.2:n.3060+83T>G
XM_011524749.1:c.2958+83T>G XP_011523051.1:n.2958+83T>G
XM_011524750.1:c.2943+388T>G XP_011523052.1:n.2943+388T>G
NM_000419.4:c.3060+83T>G NP_000410.2:n.3060+83T>G
NM_000419.5:c.3060+83T>G MANE Select NP_000410.2:n.3060+83T>G