Canonical Allele Identifier: CA399801898
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379783G>A , CM000679.2:g.44379783G>A GRCh38
NC_000017.10:g.42457151G>A , CM000679.1:g.42457151G>A GRCh37
NC_000017.9:g.39812677G>A NCBI36
NG_008331.1:g.14723C>T , LRG_479:g.14723C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1784C>T MANE Select ENSP00000262407.5:p.Pro595Leu
ENST00000648408.1:c.1215C>T
ENST00000262407.5:c.1784C>T ENSP00000262407.5:p.Pro595Leu
ENST00000592462.5:n.579C>T
NM_000419.3:c.1784C>T , LRG_479t1:c.1784C>T NP_000410.2:p.Pro595Leu
XM_011524749.1:c.1784C>T XP_011523051.1:p.Pro595Leu
XM_011524750.1:c.1784C>T XP_011523052.1:p.Pro595Leu
NM_000419.4:c.1784C>T NP_000410.2:p.Pro595Leu
NM_000419.5:c.1784C>T MANE Select NP_000410.2:p.Pro595Leu