Canonical Allele Identifier: CA1601249836

Gene: SH3PXD2B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172333403A= , CM000667.2:g.172333403A=	GRCh38
NC_000005.9:g.171760407A= , CM000667.1:g.171760407A=	GRCh37
NC_000005.8:g.171693012A=	NCBI36
NG_027746.1:g.126121T=
NG_027746.2:g.126121T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636523.1:c.1229-8023T=
ENST00000519643.5:c.1189-8023T=	ENSP00000430890.1:n.1189-8023T=
NM_001308175.1:c.1189-8023T=	NP_001295104.1:n.1189-8023T=
NM_001308175.2:c.1189-8023T=	NP_001295104.1:n.1189-8023T=