Canonical Allele Identifier: CA383982039
Gene: PLBD1 HGNC NCBI

Linked Data

dbSNP Id: rs759241417
gnomAD v4: 12-14506989-C-A
MyVariant Identifiers: chr12:g.14659923C>A (hg19) chr12:g.14506989C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506989C>A , CM000674.2:g.14506989C>A GRCh38
NC_000012.11:g.14659923C>A , CM000674.1:g.14659923C>A GRCh37
NC_000012.10:g.14551190C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1316G>T MANE Select ENSP00000240617.5:p.Arg439Leu
ENST00000240617.9:c.1316G>T ENSP00000240617.5:p.Arg439Leu
NM_024829.5:c.1316G>T NP_079105.4:p.Arg439Leu
NM_024829.6:c.1316G>T MANE Select NP_079105.4:p.Arg439Leu
Search 100 bp 5'
Search 100 bp 3'