Canonical Allele Identifier: CA2638215312
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44375291-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375291T>G , CM000679.2:g.44375291T>G GRCh38
NC_000017.10:g.42452659T>G , CM000679.1:g.42452659T>G GRCh37
NC_000017.9:g.39808185T>G NCBI36
NG_008331.1:g.19215A>C , LRG_479:g.19215A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2728-180A>C MANE Select ENSP00000262407.5:n.2728-180A>C
ENST00000648408.1:c.2159-180A>C
ENST00000262407.5:c.2728-180A>C ENSP00000262407.5:n.2728-180A>C
ENST00000587295.5:c.253+542A>C
ENST00000592462.5:n.1822A>C
NM_000419.3:c.2728-180A>C , LRG_479t1:c.2728-180A>C NP_000410.2:n.2728-180A>C
XM_011524749.1:c.2728-180A>C XP_011523051.1:n.2728-180A>C
XM_011524750.1:c.2728-180A>C XP_011523052.1:n.2728-180A>C
NM_000419.4:c.2728-180A>C NP_000410.2:n.2728-180A>C
NM_000419.5:c.2728-180A>C MANE Select NP_000410.2:n.2728-180A>C
Search 100 bp 5'
Search 100 bp 3'