Canonical Allele Identifier: CA2676498494
Gene: SH3PXD2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333415T>C , CM000667.2:g.172333415T>C GRCh38
NC_000005.9:g.171760419T>C , CM000667.1:g.171760419T>C GRCh37
NC_000005.8:g.171693024T>C NCBI36
NG_027746.1:g.126109A>G
NG_027746.2:g.126109A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000636523.1:c.1229-8035A>G
ENST00000519643.5:c.1189-8035A>G ENSP00000430890.1:n.1189-8035A>G
NM_001308175.1:c.1189-8035A>G NP_001295104.1:n.1189-8035A>G
NM_001308175.2:c.1189-8035A>G NP_001295104.1:n.1189-8035A>G