Canonical Allele Identifier: CA399792804
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42452972T>C (hg19) chr17:g.44375604T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375604T>C , CM000679.2:g.44375604T>C GRCh38
NC_000017.10:g.42452972T>C , CM000679.1:g.42452972T>C GRCh37
NC_000017.9:g.39808498T>C NCBI36
NG_008331.1:g.18902A>G , LRG_479:g.18902A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2714A>G MANE Select ENSP00000262407.5:p.Asp905Gly
ENST00000648408.1:c.2145A>G
ENST00000262407.5:c.2714A>G ENSP00000262407.5:p.Asp905Gly
ENST00000587295.5:c.253+229A>G
ENST00000592462.5:n.1509A>G
NM_000419.3:c.2714A>G , LRG_479t1:c.2714A>G NP_000410.2:p.Asp905Gly
XM_011524749.1:c.2714A>G XP_011523051.1:p.Asp905Gly
XM_011524750.1:c.2714A>G XP_011523052.1:p.Asp905Gly
NM_000419.4:c.2714A>G NP_000410.2:p.Asp905Gly
NM_000419.5:c.2714A>G MANE Select NP_000410.2:p.Asp905Gly
Search 100 bp 5'
Search 100 bp 3'