Canonical Allele Identifier: CA383982050
Gene: PLBD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.14659929A>T (hg19) chr12:g.14506995A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506995A>T , CM000674.2:g.14506995A>T GRCh38
NC_000012.11:g.14659929A>T , CM000674.1:g.14659929A>T GRCh37
NC_000012.10:g.14551196A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1310T>A MANE Select ENSP00000240617.5:p.Phe437Tyr
ENST00000240617.9:c.1310T>A ENSP00000240617.5:p.Phe437Tyr
NM_024829.5:c.1310T>A NP_079105.4:p.Phe437Tyr
NM_024829.6:c.1310T>A MANE Select NP_079105.4:p.Phe437Tyr
Search 100 bp 5'
Search 100 bp 3'