Canonical Allele Identifier: CA383981976

Gene: PLBD1

Linked Data

• MyVariant Identifiers: chr12:g.14659893G>C (hg19) ; chr12:g.14506959G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14506959G>C , CM000674.2:g.14506959G>C	GRCh38
NC_000012.11:g.14659893G>C , CM000674.1:g.14659893G>C	GRCh37
NC_000012.10:g.14551160G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240617.10:c.1346C>G MANE Select	ENSP00000240617.5:p.Ser449Cys
ENST00000240617.9:c.1346C>G	ENSP00000240617.5:p.Ser449Cys
NM_024829.5:c.1346C>G	NP_079105.4:p.Ser449Cys
NM_024829.6:c.1346C>G MANE Select	NP_079105.4:p.Ser449Cys