Canonical Allele Identifier: CA1601249925
Gene: SH3PXD2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333464T= , CM000667.2:g.172333464T= GRCh38
NC_000005.9:g.171760468T= , CM000667.1:g.171760468T= GRCh37
NC_000005.8:g.171693073T= NCBI36
NG_027746.1:g.126060A=
NG_027746.2:g.126060A=

Transcript Alleles

HGVS Amino-acid change
ENST00000636523.1:c.1229-8084A=
ENST00000519643.5:c.1189-8084A= ENSP00000430890.1:n.1189-8084A=
NM_001308175.1:c.1189-8084A= NP_001295104.1:n.1189-8084A=
NM_001308175.2:c.1189-8084A= NP_001295104.1:n.1189-8084A=
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