Canonical Allele Identifier: CA8603041
Community Standard Title: NM_000419.5(ITGA2B):c.1545-8C>A
Gene: ITGA2B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44380309G>T , CM000679.2:g.44380309G>T GRCh38
NC_000017.10:g.42457677G>T , CM000679.1:g.42457677G>T GRCh37
NC_000017.9:g.39813203G>T NCBI36
NG_008331.1:g.14197C>A , LRG_479:g.14197C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000419.5:c.1545-8C>A MANE Select NP_000410.2:n.1545-8C>A
ENST00000262407.6:c.1545-8C>A MANE Select ENSP00000262407.5:n.1545-8C>A
NM_000419.3:c.1545-8C>A , LRG_479t1:c.1545-8C>A NP_000410.2:n.1545-8C>A
NM_000419.4:c.1545-8C>A NP_000410.2:n.1545-8C>A
ENST00000262407.5:c.1545-8C>A ENSP00000262407.5:n.1545-8C>A
ENST00000592226.5:n.1018-8C>A
ENST00000592462.5:n.340-8C>A
ENST00000648408.1:c.976-8C>A
XM_011524749.1:c.1545-8C>A XP_011523051.1:n.1545-8C>A
XM_011524750.1:c.1545-8C>A XP_011523052.1:n.1545-8C>A
Search 100 bp 5'
Search 100 bp 3'