Canonical Allele Identifier: CA415101740

Gene: PLXNB3

Linked Data

• MyVariant Identifiers: chrX:g.153035670C>T (hg19) ; chrX:g.153770215C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770215C>T , CM000685.2:g.153770215C>T	GRCh38
NC_000023.10:g.153035670C>T , CM000685.1:g.153035670C>T	GRCh37
NC_000023.9:g.152688864C>T	NCBI36
NG_013255.1:g.11020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1753C>T MANE Select	ENSP00000355378.5:p.Gln585Ter
ENST00000361971.9:c.1753C>T	ENSP00000355378.5:p.Gln585Ter
ENST00000538966.5:c.1822C>T	ENSP00000442736.1:p.Gln608Ter
NM_001163257.1:c.1822C>T	NP_001156729.1:p.Gln608Ter
NM_005393.2:c.1753C>T	NP_005384.2:p.Gln585Ter
NM_005393.3:c.1753C>T MANE Select	NP_005384.2:p.Gln585Ter
NM_001163257.2:c.1822C>T	NP_001156729.1:p.Gln608Ter