Canonical Allele Identifier: CA983996307

Gene: ITGA2B

Linked Data

• gnomAD v3: 17-44377689-C-CTTTTTT
• gnomAD v4: 17-44377689-C-CTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377689_44377690insTTTTTT , CM000679.2:g.44377689_44377690insTTTTTT	GRCh38
NC_000017.10:g.42455057_42455058insTTTTTT , CM000679.1:g.42455057_42455058insTTTTTT	GRCh37
NC_000017.9:g.39810583_39810584insTTTTTT	NCBI36
NG_008331.1:g.16816_16817insAAAAAA , LRG_479:g.16816_16817insAAAAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2187+8_2187+9insAAAAAA MANE Select	ENSP00000262407.5:n.2187+8_2187+9insAAAAA...
ENST00000648408.1:c.1618+8_1618+9insAAAAAA
ENST00000262407.5:c.2187+8_2187+9insAAAAAA	ENSP00000262407.5:n.2187+8_2187+9insAAAAA...
ENST00000592462.5:n.982+8_982+9insAAAAAA
NM_000419.3:c.2187+8_2187+9insAAAAAA , LRG_479t1:c.2187+8_2187+9insAAAAAA	NP_000410.2:n.2187+8_2187+9insAAAAAA
XM_011524749.1:c.2187+8_2187+9insAAAAAA	XP_011523051.1:n.2187+8_2187+9insAAAAAA
XM_011524750.1:c.2187+8_2187+9insAAAAAA	XP_011523052.1:n.2187+8_2187+9insAAAAAA
NM_000419.4:c.2187+8_2187+9insAAAAAA	NP_000410.2:n.2187+8_2187+9insAAAAAA
NM_000419.5:c.2187+8_2187+9insAAAAAA MANE Select	NP_000410.2:n.2187+8_2187+9insAAAAAA