Canonical Allele Identifier: CA415101476
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs782708590
gnomAD v2: X-153035613-G-T
gnomAD v4: X-153770158-G-T
MyVariant Identifiers: chrX:g.153035613G>T (hg19) chrX:g.153770158G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770158G>T , CM000685.2:g.153770158G>T GRCh38
NC_000023.10:g.153035613G>T , CM000685.1:g.153035613G>T GRCh37
NC_000023.9:g.152688807G>T NCBI36
NG_013255.1:g.10963G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1696G>T MANE Select ENSP00000355378.5:p.Asp566Tyr
ENST00000361971.9:c.1696G>T ENSP00000355378.5:p.Asp566Tyr
ENST00000538966.5:c.1765G>T ENSP00000442736.1:p.Asp589Tyr
NM_001163257.1:c.1765G>T NP_001156729.1:p.Asp589Tyr
NM_005393.2:c.1696G>T NP_005384.2:p.Asp566Tyr
NM_005393.3:c.1696G>T MANE Select NP_005384.2:p.Asp566Tyr
NM_001163257.2:c.1765G>T NP_001156729.1:p.Asp589Tyr
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