Canonical Allele Identifier: CA2466468339

Gene: PLXNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770150C= , CM000685.2:g.153770150C=	GRCh38
NC_000023.10:g.153035605C= , CM000685.1:g.153035605C=	GRCh37
NC_000023.9:g.152688799C=	NCBI36
NG_013255.1:g.10955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1688C= MANE Select	ENSP00000355378.5:p.Ala563=
ENST00000361971.9:c.1688C=	ENSP00000355378.5:p.Ala563=
ENST00000538966.5:c.1757C=	ENSP00000442736.1:p.Ala586=
NM_001163257.1:c.1757C=	NP_001156729.1:p.Ala586=
NM_005393.2:c.1688C=	NP_005384.2:p.Ala563=
NM_005393.3:c.1688C= MANE Select	NP_005384.2:p.Ala563=
NM_001163257.2:c.1757C=	NP_001156729.1:p.Ala586=