Canonical Allele Identifier: CA2466468428
Gene: PLXNB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770323A= , CM000685.2:g.153770323A= GRCh38
NC_000023.10:g.153035778A= , CM000685.1:g.153035778A= GRCh37
NC_000023.9:g.152688972A= NCBI36
NG_013255.1:g.11128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1787-15A= MANE Select ENSP00000355378.5:n.1787-15A=
ENST00000361971.9:c.1787-15A= ENSP00000355378.5:n.1787-15A=
ENST00000538966.5:c.1856-15A= ENSP00000442736.1:n.1856-15A=
NM_001163257.1:c.1856-15A= NP_001156729.1:n.1856-15A=
NM_005393.2:c.1787-15A= NP_005384.2:n.1787-15A=
NM_005393.3:c.1787-15A= MANE Select NP_005384.2:n.1787-15A=
NM_001163257.2:c.1856-15A= NP_001156729.1:n.1856-15A=
Search 100 bp 5'
Search 100 bp 3'