Canonical Allele Identifier: CA2638214895
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44374837-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374837C>G , CM000679.2:g.44374837C>G GRCh38
NC_000017.10:g.42452205C>G , CM000679.1:g.42452205C>G GRCh37
NC_000017.9:g.39807731C>G NCBI36
NG_008331.1:g.19669G>C , LRG_479:g.19669G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2842-77G>C MANE Select ENSP00000262407.5:n.2842-77G>C
ENST00000648408.1:c.2273-77G>C
ENST00000262407.5:c.2842-77G>C ENSP00000262407.5:n.2842-77G>C
ENST00000587295.5:c.253+996G>C
ENST00000592462.5:n.2276G>C
NM_000419.3:c.2842-77G>C , LRG_479t1:c.2842-77G>C NP_000410.2:n.2842-77G>C
XM_011524749.1:c.2841+161G>C XP_011523051.1:n.2841+161G>C
XM_011524750.1:c.2842-77G>C XP_011523052.1:n.2842-77G>C
NM_000419.4:c.2842-77G>C NP_000410.2:n.2842-77G>C
NM_000419.5:c.2842-77G>C MANE Select NP_000410.2:n.2842-77G>C
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