Canonical Allele Identifier: CA1601249873
Gene: SH3PXD2B HGNC NCBI

Linked Data

dbSNP Id: rs1756606319
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333435A>T , CM000667.2:g.172333435A>T GRCh38
NC_000005.9:g.171760439A>T , CM000667.1:g.171760439A>T GRCh37
NC_000005.8:g.171693044A>T NCBI36
NG_027746.1:g.126089T>A
NG_027746.2:g.126089T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636523.1:c.1229-8055T>A
ENST00000519643.5:c.1189-8055T>A ENSP00000430890.1:n.1189-8055T>A
NM_001308175.1:c.1189-8055T>A NP_001295104.1:n.1189-8055T>A
NM_001308175.2:c.1189-8055T>A NP_001295104.1:n.1189-8055T>A
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