Canonical Allele Identifier: CA888563

Gene: ITGB3BP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63454895T>C , CM000663.2:g.63454895T>C	GRCh38
NC_000001.10:g.63920566T>C , CM000663.1:g.63920566T>C	GRCh37
NC_000001.9:g.63693154T>C	NCBI36
NG_030011.1:g.73379A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271002.15:c.328A>G MANE Select	ENSP00000271002.10:p.Ile110Val
ENST00000271002.14:c.328A>G	ENSP00000271002.10:p.Ile110Val
ENST00000371092.7:c.445A>G	ENSP00000360133.3:p.Ile149Val
ENST00000460394.5:n.377A>G
ENST00000461681.5:n.636A>G
ENST00000462285.5:n.198A>G
ENST00000463803.5:n.55A>G
ENST00000476508.5:n.276A>G
ENST00000489099.5:c.328A>G	ENSP00000432904.1:p.Ile110Val
ENST00000489863.5:n.407A>G
NM_001206739.1:c.445A>G	NP_001193668.1:p.Ile149Val
NM_014288.4:c.328A>G	NP_055103.3:p.Ile110Val
NR_045147.1:n.468A>G
XM_006710514.2:c.328A>G	XP_006710577.2:p.Ile110Val
XM_006710515.2:c.328A>G	XP_006710578.2:p.Ile110Val
XM_011541131.1:c.208A>G	XP_011539433.1:p.Ile70Val
NM_001347145.1:c.328A>G	NP_001334074.1:p.Ile110Val
NM_001347147.1:c.328A>G	NP_001334076.1:p.Ile110Val
NM_001347148.1:c.208A>G	NP_001334077.1:p.Ile70Val
XM_017000853.2:c.328A>G	XP_016856342.2:p.Ile110Val
XM_017000854.2:c.208A>G	XP_016856343.2:p.Ile70Val
XM_017000855.2:c.430A>G	XP_016856344.1:p.Ile144Val
XM_024446041.1:c.430A>G	XP_024301809.1:p.Ile144Val
XM_024446042.1:c.208A>G	XP_024301810.1:p.Ile70Val
NM_001206739.2:c.445A>G	NP_001193668.1:p.Ile149Val
NM_001347145.2:c.328A>G	NP_001334074.1:p.Ile110Val
NM_001347147.2:c.328A>G	NP_001334076.1:p.Ile110Val
NM_001347148.2:c.208A>G	NP_001334077.1:p.Ile70Val
NM_014288.5:c.328A>G MANE Select	NP_055103.3:p.Ile110Val
NR_045147.2:n.420A>G