Canonical Allele Identifier: CA10550948
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs781918801
ExAC: X:153035772 GC / G
gnomAD v2: X-153035772-GC-G
gnomAD v3: X-153770317-GC-G
gnomAD v4: X-153770317-GC-G
MyVariant Identifiers: chrX:g.153035773del (hg19) chrX:g.153770318del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770322del , CM000685.2:g.153770322del GRCh38
NC_000023.10:g.153035777del , CM000685.1:g.153035777del GRCh37
NC_000023.9:g.152688971del NCBI36
NG_013255.1:g.11127del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1787-16del MANE Select ENSP00000355378.5:n.1787-16del
ENST00000361971.9:c.1787-16del ENSP00000355378.5:n.1787-16del
ENST00000538966.5:c.1856-16del ENSP00000442736.1:n.1856-16del
NM_001163257.1:c.1856-16del NP_001156729.1:n.1856-16del
NM_005393.2:c.1787-16del NP_005384.2:n.1787-16del
NM_005393.3:c.1787-16del MANE Select NP_005384.2:n.1787-16del
NM_001163257.2:c.1856-16del NP_001156729.1:n.1856-16del
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