Canonical Allele Identifier: CA13614689
Gene: PLBD1 HGNC NCBI

Linked Data

dbSNP Id: rs12825370

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506874G>C , CM000674.2:g.14506874G>C GRCh38
NC_000012.11:g.14659808G>C , CM000674.1:g.14659808G>C GRCh37
NC_000012.10:g.14551075G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1372+59C>G MANE Select ENSP00000240617.5:n.1372+59C>G
ENST00000240617.9:c.1372+59C>G ENSP00000240617.5:n.1372+59C>G
NM_024829.5:c.1372+59C>G NP_079105.4:n.1372+59C>G
NM_024829.6:c.1372+59C>G MANE Select NP_079105.4:n.1372+59C>G