Canonical Allele Identifier: CA383982022

Gene: PLBD1

Linked Data

• MyVariant Identifiers: chr12:g.14659915C>G (hg19) ; chr12:g.14506981C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14506981C>G , CM000674.2:g.14506981C>G	GRCh38
NC_000012.11:g.14659915C>G , CM000674.1:g.14659915C>G	GRCh37
NC_000012.10:g.14551182C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240617.10:c.1324G>C MANE Select	ENSP00000240617.5:p.Gly442Arg
ENST00000240617.9:c.1324G>C	ENSP00000240617.5:p.Gly442Arg
NM_024829.5:c.1324G>C	NP_079105.4:p.Gly442Arg
NM_024829.6:c.1324G>C MANE Select	NP_079105.4:p.Gly442Arg