Canonical Allele Identifier: CA1601249903
Gene: SH3PXD2B HGNC NCBI

Linked Data

dbSNP Id: rs1756607295

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333456del , CM000667.2:g.172333456del GRCh38
NC_000005.9:g.171760460del , CM000667.1:g.171760460del GRCh37
NC_000005.8:g.171693065del NCBI36
NG_027746.1:g.126068del
NG_027746.2:g.126068del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636523.1:c.1229-8076del
ENST00000519643.5:c.1189-8076del ENSP00000430890.1:n.1189-8076del
NM_001308175.1:c.1189-8076del NP_001295104.1:n.1189-8076del
NM_001308175.2:c.1189-8076del NP_001295104.1:n.1189-8076del