Canonical Allele Identifier: CA2466468377
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs2091911680
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770243del , CM000685.2:g.153770243del GRCh38
NC_000023.10:g.153035698del , CM000685.1:g.153035698del GRCh37
NC_000023.9:g.152688892del NCBI36
NG_013255.1:g.11048del

Transcript Alleles

HGVS Amino-acid change
ENST00000361971.10:c.1781del MANE Select ENSP00000355378.5:p.Gly594AlafsTer11
ENST00000361971.9:c.1781del ENSP00000355378.5:p.Gly594AlafsTer11
ENST00000538966.5:c.1850del ENSP00000442736.1:p.Gly617AlafsTer11
NM_001163257.1:c.1850del NP_001156729.1:p.Gly617AlafsTer11
NM_005393.2:c.1781del NP_005384.2:p.Gly594AlafsTer11
NM_005393.3:c.1781del MANE Select NP_005384.2:p.Gly594AlafsTer11
NM_001163257.2:c.1850del NP_001156729.1:p.Gly617AlafsTer11
Search 100 bp 5'
Search 100 bp 3'