Canonical Allele Identifier: CA10550922
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs782455705

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770233A>G , CM000685.2:g.153770233A>G GRCh38
NC_000023.10:g.153035688A>G , CM000685.1:g.153035688A>G GRCh37
NC_000023.9:g.152688882A>G NCBI36
NG_013255.1:g.11038A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1771A>G MANE Select ENSP00000355378.5:p.Asn591Asp
ENST00000361971.9:c.1771A>G ENSP00000355378.5:p.Asn591Asp
ENST00000538966.5:c.1840A>G ENSP00000442736.1:p.Asn614Asp
NM_001163257.1:c.1840A>G NP_001156729.1:p.Asn614Asp
NM_005393.2:c.1771A>G NP_005384.2:p.Asn591Asp
NM_005393.3:c.1771A>G MANE Select NP_005384.2:p.Asn591Asp
NM_001163257.2:c.1840A>G NP_001156729.1:p.Asn614Asp