Canonical Allele Identifier: CA645288250

Gene: PLXNB3

Linked Data

• dbSNP Id: rs1557061216
• gnomAD v2: X-153035776-C-T
• gnomAD v4: X-153770321-C-T
• MyVariant Identifiers: chrX:g.153035776C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770321C>T , CM000685.2:g.153770321C>T	GRCh38
NC_000023.10:g.153035776C>T , CM000685.1:g.153035776C>T	GRCh37
NC_000023.9:g.152688970C>T	NCBI36
NG_013255.1:g.11126C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1787-17C>T MANE Select	ENSP00000355378.5:n.1787-17C>T
ENST00000361971.9:c.1787-17C>T	ENSP00000355378.5:n.1787-17C>T
ENST00000538966.5:c.1856-17C>T	ENSP00000442736.1:n.1856-17C>T
NM_001163257.1:c.1856-17C>T	NP_001156729.1:n.1856-17C>T
NM_005393.2:c.1787-17C>T	NP_005384.2:n.1787-17C>T
NM_005393.3:c.1787-17C>T MANE Select	NP_005384.2:n.1787-17C>T
NM_001163257.2:c.1856-17C>T	NP_001156729.1:n.1856-17C>T