Canonical Allele Identifier: CA415101669
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs1228530572

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770203G>A , CM000685.2:g.153770203G>A GRCh38
NC_000023.10:g.153035658G>A , CM000685.1:g.153035658G>A GRCh37
NC_000023.9:g.152688852G>A NCBI36
NG_013255.1:g.11008G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1741G>A MANE Select ENSP00000355378.5:p.Val581Ile
ENST00000361971.9:c.1741G>A ENSP00000355378.5:p.Val581Ile
ENST00000538966.5:c.1810G>A ENSP00000442736.1:p.Val604Ile
NM_001163257.1:c.1810G>A NP_001156729.1:p.Val604Ile
NM_005393.2:c.1741G>A NP_005384.2:p.Val581Ile
NM_005393.3:c.1741G>A MANE Select NP_005384.2:p.Val581Ile
NM_001163257.2:c.1810G>A NP_001156729.1:p.Val604Ile