Canonical Allele Identifier: CA415101885

Gene: PLXNB3

Linked Data

• MyVariant Identifiers: chrX:g.153035698G>T (hg19) ; chrX:g.153770243G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770243G>T , CM000685.2:g.153770243G>T	GRCh38
NC_000023.10:g.153035698G>T , CM000685.1:g.153035698G>T	GRCh37
NC_000023.9:g.152688892G>T	NCBI36
NG_013255.1:g.11048G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361971.10:c.1781G>T MANE Select	ENSP00000355378.5:p.Gly594Val
ENST00000361971.9:c.1781G>T	ENSP00000355378.5:p.Gly594Val
ENST00000538966.5:c.1850G>T	ENSP00000442736.1:p.Gly617Val
NM_001163257.1:c.1850G>T	NP_001156729.1:p.Gly617Val
NM_005393.2:c.1781G>T	NP_005384.2:p.Gly594Val
NM_005393.3:c.1781G>T MANE Select	NP_005384.2:p.Gly594Val
NM_001163257.2:c.1850G>T	NP_001156729.1:p.Gly617Val