Canonical Allele Identifier: CA2017888480
Gene: PLBD1 HGNC NCBI

Linked Data

dbSNP Id: rs1591992772

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14507261T>C , CM000674.2:g.14507261T>C GRCh38
NC_000012.11:g.14660195T>C , CM000674.1:g.14660195T>C GRCh37
NC_000012.10:g.14551462T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000240617.10:c.1187-143A>G MANE Select ENSP00000240617.5:n.1187-143A>G
ENST00000240617.9:c.1187-143A>G ENSP00000240617.5:n.1187-143A>G
NM_024829.5:c.1187-143A>G NP_079105.4:n.1187-143A>G
NM_024829.6:c.1187-143A>G MANE Select NP_079105.4:n.1187-143A>G