Canonical Allele Identifier: CA645288241
Gene: PLXNB3 HGNC NCBI

Linked Data

dbSNP Id: rs1339196984
gnomAD v2: X-153035726-G-A
gnomAD v3: X-153770271-G-A
gnomAD v4: X-153770271-G-A
MyVariant Identifiers: chrX:g.153035726G>A (hg19) chrX:g.153770271G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153770271G>A , CM000685.2:g.153770271G>A GRCh38
NC_000023.10:g.153035726G>A , CM000685.1:g.153035726G>A GRCh37
NC_000023.9:g.152688920G>A NCBI36
NG_013255.1:g.11076G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361971.10:c.1786+23G>A MANE Select ENSP00000355378.5:n.1786+23G>A
ENST00000361971.9:c.1786+23G>A ENSP00000355378.5:n.1786+23G>A
ENST00000538966.5:c.1855+23G>A ENSP00000442736.1:n.1855+23G>A
NM_001163257.1:c.1855+23G>A NP_001156729.1:n.1855+23G>A
NM_005393.2:c.1786+23G>A NP_005384.2:n.1786+23G>A
NM_005393.3:c.1786+23G>A MANE Select NP_005384.2:n.1786+23G>A
NM_001163257.2:c.1855+23G>A NP_001156729.1:n.1855+23G>A
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