Canonical Allele Identifier: CA415101842

Gene: PLXNB3

Linked Data

• MyVariant Identifiers: chrX:g.153035689A>T (hg19) ; chrX:g.153770234A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770234A>T , CM000685.2:g.153770234A>T	GRCh38
NC_000023.10:g.153035689A>T , CM000685.1:g.153035689A>T	GRCh37
NC_000023.9:g.152688883A>T	NCBI36
NG_013255.1:g.11039A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1772A>T MANE Select	ENSP00000355378.5:p.Asn591Ile
ENST00000361971.9:c.1772A>T	ENSP00000355378.5:p.Asn591Ile
ENST00000538966.5:c.1841A>T	ENSP00000442736.1:p.Asn614Ile
NM_001163257.1:c.1841A>T	NP_001156729.1:p.Asn614Ile
NM_005393.2:c.1772A>T	NP_005384.2:p.Asn591Ile
NM_005393.3:c.1772A>T MANE Select	NP_005384.2:p.Asn591Ile
NM_001163257.2:c.1841A>T	NP_001156729.1:p.Asn614Ile