Canonical Allele Identifier: CA415101750
Gene: PLXNB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153035672A>C (hg19) chrX:g.153770217A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770217A>C , CM000685.2:g.153770217A>C GRCh38
NC_000023.10:g.153035672A>C , CM000685.1:g.153035672A>C GRCh37
NC_000023.9:g.152688866A>C NCBI36
NG_013255.1:g.11022A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1755A>C MANE Select ENSP00000355378.5:p.Gln585His
ENST00000361971.9:c.1755A>C ENSP00000355378.5:p.Gln585His
ENST00000538966.5:c.1824A>C ENSP00000442736.1:p.Gln608His
NM_001163257.1:c.1824A>C NP_001156729.1:p.Gln608His
NM_005393.2:c.1755A>C NP_005384.2:p.Gln585His
NM_005393.3:c.1755A>C MANE Select NP_005384.2:p.Gln585His
NM_001163257.2:c.1824A>C NP_001156729.1:p.Gln608His
Search 100 bp 5'
Search 100 bp 3'