Canonical Allele Identifier: CA383981935
Gene: PLBD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506942G>C , CM000674.2:g.14506942G>C GRCh38
NC_000012.11:g.14659876G>C , CM000674.1:g.14659876G>C GRCh37
NC_000012.10:g.14551143G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1363C>G MANE Select ENSP00000240617.5:p.Arg455Gly
ENST00000240617.9:c.1363C>G ENSP00000240617.5:p.Arg455Gly
NM_024829.5:c.1363C>G NP_079105.4:p.Arg455Gly
NM_024829.6:c.1363C>G MANE Select NP_079105.4:p.Arg455Gly