Canonical Allele Identifier: CA8602620
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs751616204
ExAC: 17:42452970 G / A
gnomAD v2: 17-42452970-G-A
gnomAD v3: 17-44375602-G-A
gnomAD v4: 17-44375602-G-A
MyVariant Identifiers: chr17:g.42452970G>A (hg19) chr17:g.44375602G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375602G>A , CM000679.2:g.44375602G>A GRCh38
NC_000017.10:g.42452970G>A , CM000679.1:g.42452970G>A GRCh37
NC_000017.9:g.39808496G>A NCBI36
NG_008331.1:g.18904C>T , LRG_479:g.18904C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2716C>T MANE Select ENSP00000262407.5:p.Pro906Ser
ENST00000648408.1:c.2147C>T
ENST00000262407.5:c.2716C>T ENSP00000262407.5:p.Pro906Ser
ENST00000587295.5:c.253+231C>T
ENST00000592462.5:n.1511C>T
NM_000419.3:c.2716C>T , LRG_479t1:c.2716C>T NP_000410.2:p.Pro906Ser
XM_011524749.1:c.2716C>T XP_011523051.1:p.Pro906Ser
XM_011524750.1:c.2716C>T XP_011523052.1:p.Pro906Ser
NM_000419.4:c.2716C>T NP_000410.2:p.Pro906Ser
NM_000419.5:c.2716C>T MANE Select NP_000410.2:p.Pro906Ser
Search 100 bp 5'
Search 100 bp 3'