Canonical Allele Identifier: CA519347346

Gene: PLXNB3

Linked Data

• MyVariant Identifiers: chrX:g.153035884C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770429C>G , CM000685.2:g.153770429C>G	GRCh38
NC_000023.10:g.153035884C>G , CM000685.1:g.153035884C>G	GRCh37
NC_000023.9:g.152689078C>G	NCBI36
NG_013255.1:g.11234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1878C>G MANE Select	ENSP00000355378.5:p.Ala626=
ENST00000361971.9:c.1878C>G	ENSP00000355378.5:p.Ala626=
ENST00000538966.5:c.1947C>G	ENSP00000442736.1:p.Ala649=
NM_001163257.1:c.1947C>G	NP_001156729.1:p.Ala649=
NM_005393.2:c.1878C>G	NP_005384.2:p.Ala626=
NM_005393.3:c.1878C>G MANE Select	NP_005384.2:p.Ala626=
NM_001163257.2:c.1947C>G	NP_001156729.1:p.Ala649=