Canonical Allele Identifier: CA10550958
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs782119991
ExAC: X:153035824 C / T
gnomAD v2: X-153035824-C-T
gnomAD v3: X-153770369-C-T
gnomAD v4: X-153770369-C-T
COSMIC: COSM1117497 COSM1599029
MyVariant Identifiers: chrX:g.153035824C>T (hg19) chrX:g.153770369C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770369C>T , CM000685.2:g.153770369C>T GRCh38
NC_000023.10:g.153035824C>T , CM000685.1:g.153035824C>T GRCh37
NC_000023.9:g.152689018C>T NCBI36
NG_013255.1:g.11174C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1818C>T MANE Select ENSP00000355378.5:p.Phe606=
ENST00000361971.9:c.1818C>T ENSP00000355378.5:p.Phe606=
ENST00000538966.5:c.1887C>T ENSP00000442736.1:p.Phe629=
NM_001163257.1:c.1887C>T NP_001156729.1:p.Phe629=
NM_005393.2:c.1818C>T NP_005384.2:p.Phe606=
NM_005393.3:c.1818C>T MANE Select NP_005384.2:p.Phe606=
NM_001163257.2:c.1887C>T NP_001156729.1:p.Phe629=
Search 100 bp 5'
Search 100 bp 3'