Canonical Allele Identifier: CA2017888299
Gene: PLBD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506899T= , CM000674.2:g.14506899T= GRCh38
NC_000012.11:g.14659833T= , CM000674.1:g.14659833T= GRCh37
NC_000012.10:g.14551100T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1372+34A= MANE Select ENSP00000240617.5:n.1372+34A=
ENST00000240617.9:c.1372+34A= ENSP00000240617.5:n.1372+34A=
NM_024829.5:c.1372+34A= NP_079105.4:n.1372+34A=
NM_024829.6:c.1372+34A= MANE Select NP_079105.4:n.1372+34A=