Canonical Allele Identifier: CA1601249909
Gene: SH3PXD2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333458T= , CM000667.2:g.172333458T= GRCh38
NC_000005.9:g.171760462T= , CM000667.1:g.171760462T= GRCh37
NC_000005.8:g.171693067T= NCBI36
NG_027746.1:g.126066A=
NG_027746.2:g.126066A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636523.1:c.1229-8078A=
ENST00000519643.5:c.1189-8078A= ENSP00000430890.1:n.1189-8078A=
NM_001308175.1:c.1189-8078A= NP_001295104.1:n.1189-8078A=
NM_001308175.2:c.1189-8078A= NP_001295104.1:n.1189-8078A=