Canonical Allele Identifier: CA2466468382
Gene: PLXNB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770251G= , CM000685.2:g.153770251G= GRCh38
NC_000023.10:g.153035706G= , CM000685.1:g.153035706G= GRCh37
NC_000023.9:g.152688900G= NCBI36
NG_013255.1:g.11056G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361971.10:c.1786+3G= MANE Select ENSP00000355378.5:n.1786+3G=
ENST00000361971.9:c.1786+3G= ENSP00000355378.5:n.1786+3G=
ENST00000538966.5:c.1855+3G= ENSP00000442736.1:n.1855+3G=
NM_001163257.1:c.1855+3G= NP_001156729.1:n.1855+3G=
NM_005393.2:c.1786+3G= NP_005384.2:n.1786+3G=
NM_005393.3:c.1786+3G= MANE Select NP_005384.2:n.1786+3G=
NM_001163257.2:c.1855+3G= NP_001156729.1:n.1855+3G=
Search 100 bp 5'
Search 100 bp 3'