Canonical Allele Identifier: CA290954433

Gene: ITGA2B

Linked Data

• dbSNP Id: rs985354820
• MyVariant Identifiers: chr17:g.42461585G>A (hg19) ; chr17:g.44384217G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384217G>A , CM000679.2:g.44384217G>A	GRCh38
NC_000017.10:g.42461585G>A , CM000679.1:g.42461585G>A	GRCh37
NC_000017.9:g.39817111G>A	NCBI36
NG_008331.1:g.10289C>T , LRG_479:g.10289C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.892-79C>T MANE Select	ENSP00000262407.5:n.892-79C>T
ENST00000648408.1:c.323-79C>T
ENST00000262407.5:c.892-79C>T	ENSP00000262407.5:n.892-79C>T
ENST00000589645.5:n.343-79C>T
ENST00000591990.5:n.437-79C>T
ENST00000592075.5:n.261-79C>T
ENST00000592226.5:n.132-79C>T
ENST00000592253.5:n.400-79C>T
NM_000419.3:c.892-79C>T , LRG_479t1:c.892-79C>T	NP_000410.2:n.892-79C>T
XM_011524749.1:c.892-79C>T	XP_011523051.1:n.892-79C>T
XM_011524750.1:c.892-79C>T	XP_011523052.1:n.892-79C>T
NM_000419.4:c.892-79C>T	NP_000410.2:n.892-79C>T
NM_000419.5:c.892-79C>T MANE Select	NP_000410.2:n.892-79C>T