Canonical Allele Identifier: CA415101499

Gene: PLXNB3

Linked Data

• gnomAD v4: X-153770162-A-G
• MyVariant Identifiers: chrX:g.153035617A>G (hg19) ; chrX:g.153770162A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770162A>G , CM000685.2:g.153770162A>G	GRCh38
NC_000023.10:g.153035617A>G , CM000685.1:g.153035617A>G	GRCh37
NC_000023.9:g.152688811A>G	NCBI36
NG_013255.1:g.10967A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1700A>G MANE Select	ENSP00000355378.5:p.Tyr567Cys
ENST00000361971.9:c.1700A>G	ENSP00000355378.5:p.Tyr567Cys
ENST00000538966.5:c.1769A>G	ENSP00000442736.1:p.Tyr590Cys
NM_001163257.1:c.1769A>G	NP_001156729.1:p.Tyr590Cys
NM_005393.2:c.1700A>G	NP_005384.2:p.Tyr567Cys
NM_005393.3:c.1700A>G MANE Select	NP_005384.2:p.Tyr567Cys
NM_001163257.2:c.1769A>G	NP_001156729.1:p.Tyr590Cys