Canonical Allele Identifier: CA415101916

Gene: PLXNB3

Linked Data

• dbSNP Id: rs1168418120
• gnomAD v3: X-153770249-G-A
• gnomAD v4: X-153770249-G-A
• MyVariant Identifiers: chrX:g.153035704G>A (hg19) ; chrX:g.153770249G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770249G>A , CM000685.2:g.153770249G>A	GRCh38
NC_000023.10:g.153035704G>A , CM000685.1:g.153035704G>A	GRCh37
NC_000023.9:g.152688898G>A	NCBI36
NG_013255.1:g.11054G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361971.10:c.1786+1G>A MANE Select	ENSP00000355378.5:n.1786+1G>A
ENST00000361971.9:c.1786+1G>A	ENSP00000355378.5:n.1786+1G>A
ENST00000538966.5:c.1855+1G>A	ENSP00000442736.1:n.1855+1G>A
NM_001163257.1:c.1855+1G>A	NP_001156729.1:n.1855+1G>A
NM_005393.2:c.1786+1G>A	NP_005384.2:n.1786+1G>A
NM_005393.3:c.1786+1G>A MANE Select	NP_005384.2:n.1786+1G>A
NM_001163257.2:c.1855+1G>A	NP_001156729.1:n.1855+1G>A