Canonical Allele Identifier: CA519347076

Gene: PLXNB3

Linked Data

• dbSNP Id: rs1557061139
• gnomAD v2: X-153035651-G-T
• MyVariant Identifiers: chrX:g.153035651G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770196G>T , CM000685.2:g.153770196G>T	GRCh38
NC_000023.10:g.153035651G>T , CM000685.1:g.153035651G>T	GRCh37
NC_000023.9:g.152688845G>T	NCBI36
NG_013255.1:g.11001G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1734G>T MANE Select	ENSP00000355378.5:p.Val578=
ENST00000361971.9:c.1734G>T	ENSP00000355378.5:p.Val578=
ENST00000538966.5:c.1803G>T	ENSP00000442736.1:p.Val601=
NM_001163257.1:c.1803G>T	NP_001156729.1:p.Val601=
NM_005393.2:c.1734G>T	NP_005384.2:p.Val578=
NM_005393.3:c.1734G>T MANE Select	NP_005384.2:p.Val578=
NM_001163257.2:c.1803G>T	NP_001156729.1:p.Val601=