Canonical Allele Identifier: CA415101559

Gene: PLXNB3

Linked Data

• MyVariant Identifiers: chrX:g.153035633T>G (hg19) ; chrX:g.153770178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770178T>G , CM000685.2:g.153770178T>G	GRCh38
NC_000023.10:g.153035633T>G , CM000685.1:g.153035633T>G	GRCh37
NC_000023.9:g.152688827T>G	NCBI36
NG_013255.1:g.10983T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1716T>G MANE Select	ENSP00000355378.5:p.His572Gln
ENST00000361971.9:c.1716T>G	ENSP00000355378.5:p.His572Gln
ENST00000538966.5:c.1785T>G	ENSP00000442736.1:p.His595Gln
NM_001163257.1:c.1785T>G	NP_001156729.1:p.His595Gln
NM_005393.2:c.1716T>G	NP_005384.2:p.His572Gln
NM_005393.3:c.1716T>G MANE Select	NP_005384.2:p.His572Gln
NM_001163257.2:c.1785T>G	NP_001156729.1:p.His595Gln