Canonical Allele Identifier: CA10550928
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs782364362
ExAC: X:153035715 A / G
gnomAD v2: X-153035715-A-G
gnomAD v3: X-153770260-A-G
gnomAD v4: X-153770260-A-G
MyVariant Identifiers: chrX:g.153035715A>G (hg19) chrX:g.153770260A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770260A>G , CM000685.2:g.153770260A>G GRCh38
NC_000023.10:g.153035715A>G , CM000685.1:g.153035715A>G GRCh37
NC_000023.9:g.152688909A>G NCBI36
NG_013255.1:g.11065A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361971.10:c.1786+12A>G MANE Select ENSP00000355378.5:n.1786+12A>G
ENST00000361971.9:c.1786+12A>G ENSP00000355378.5:n.1786+12A>G
ENST00000538966.5:c.1855+12A>G ENSP00000442736.1:n.1855+12A>G
NM_001163257.1:c.1855+12A>G NP_001156729.1:n.1855+12A>G
NM_005393.2:c.1786+12A>G NP_005384.2:n.1786+12A>G
NM_005393.3:c.1786+12A>G MANE Select NP_005384.2:n.1786+12A>G
NM_001163257.2:c.1855+12A>G NP_001156729.1:n.1855+12A>G
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