Canonical Allele Identifier: CA415101602
Gene: PLXNB3 HGNC NCBI

Linked Data

gnomAD v4: X-153770189-C-A
MyVariant Identifiers: chrX:g.153035644C>A (hg19) chrX:g.153770189C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770189C>A , CM000685.2:g.153770189C>A GRCh38
NC_000023.10:g.153035644C>A , CM000685.1:g.153035644C>A GRCh37
NC_000023.9:g.152688838C>A NCBI36
NG_013255.1:g.10994C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1727C>A MANE Select ENSP00000355378.5:p.Pro576His
ENST00000361971.9:c.1727C>A ENSP00000355378.5:p.Pro576His
ENST00000538966.5:c.1796C>A ENSP00000442736.1:p.Pro599His
NM_001163257.1:c.1796C>A NP_001156729.1:p.Pro599His
NM_005393.2:c.1727C>A NP_005384.2:p.Pro576His
NM_005393.3:c.1727C>A MANE Select NP_005384.2:p.Pro576His
NM_001163257.2:c.1796C>A NP_001156729.1:p.Pro599His
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