Canonical Allele Identifier: CA399806003
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42463062C>G (hg19) chr17:g.44385694C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44385694C>G , CM000679.2:g.44385694C>G GRCh38
NC_000017.10:g.42463062C>G , CM000679.1:g.42463062C>G GRCh37
NC_000017.9:g.39818588C>G NCBI36
NG_008331.1:g.8812G>C , LRG_479:g.8812G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.431G>C MANE Select ENSP00000262407.5:p.Trp144Ser
ENST00000262407.5:c.431G>C ENSP00000262407.5:p.Trp144Ser
ENST00000592944.1:n.116G>C
NM_000419.3:c.431G>C , LRG_479t1:c.431G>C NP_000410.2:p.Trp144Ser
XM_011524749.1:c.431G>C XP_011523051.1:p.Trp144Ser
XM_011524750.1:c.431G>C XP_011523052.1:p.Trp144Ser
NM_000419.4:c.431G>C NP_000410.2:p.Trp144Ser
NM_000419.5:c.431G>C MANE Select NP_000410.2:p.Trp144Ser
Search 100 bp 5'
Search 100 bp 3'