Canonical Allele Identifier: CA519346936

Gene: PLXNB3

Linked Data

• MyVariant Identifiers: chrX:g.153035612G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770157G>C , CM000685.2:g.153770157G>C	GRCh38
NC_000023.10:g.153035612G>C , CM000685.1:g.153035612G>C	GRCh37
NC_000023.9:g.152688806G>C	NCBI36
NG_013255.1:g.10962G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1695G>C MANE Select	ENSP00000355378.5:p.Gly565=
ENST00000361971.9:c.1695G>C	ENSP00000355378.5:p.Gly565=
ENST00000538966.5:c.1764G>C	ENSP00000442736.1:p.Gly588=
NM_001163257.1:c.1764G>C	NP_001156729.1:p.Gly588=
NM_005393.2:c.1695G>C	NP_005384.2:p.Gly565=
NM_005393.3:c.1695G>C MANE Select	NP_005384.2:p.Gly565=
NM_001163257.2:c.1764G>C	NP_001156729.1:p.Gly588=