Canonical Allele Identifier: CA1601249900
Gene: SH3PXD2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333454T= , CM000667.2:g.172333454T= GRCh38
NC_000005.9:g.171760458T= , CM000667.1:g.171760458T= GRCh37
NC_000005.8:g.171693063T= NCBI36
NG_027746.1:g.126070A=
NG_027746.2:g.126070A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636523.1:c.1229-8074A=
ENST00000519643.5:c.1189-8074A= ENSP00000430890.1:n.1189-8074A=
NM_001308175.1:c.1189-8074A= NP_001295104.1:n.1189-8074A=
NM_001308175.2:c.1189-8074A= NP_001295104.1:n.1189-8074A=