Canonical Allele Identifier: CA399804774

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44383933A>G , CM000679.2:g.44383933A>G	GRCh38
NC_000017.10:g.42461301A>G , CM000679.1:g.42461301A>G	GRCh37
NC_000017.9:g.39816827A>G	NCBI36
NG_008331.1:g.10573T>C , LRG_479:g.10573T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.959T>C MANE Select	NP_000410.2:p.Phe320Ser
ENST00000262407.6:c.959T>C MANE Select	ENSP00000262407.5:p.Phe320Ser
NM_000419.3:c.959T>C , LRG_479t1:c.959T>C	NP_000410.2:p.Phe320Ser
NM_000419.4:c.959T>C	NP_000410.2:p.Phe320Ser
ENST00000262407.5:c.959T>C	ENSP00000262407.5:p.Phe320Ser
ENST00000589645.5:n.410T>C
ENST00000591990.5:n.504T>C
ENST00000592226.5:n.199T>C
ENST00000648408.1:c.390T>C
XM_011524749.1:c.959T>C	XP_011523051.1:p.Phe320Ser
XM_011524750.1:c.959T>C	XP_011523052.1:p.Phe320Ser