Canonical Allele Identifier: CA944992018
Gene: PLBD1 HGNC NCBI

Linked Data

dbSNP Id: rs1945264039

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14507252T>A , CM000674.2:g.14507252T>A GRCh38
NC_000012.11:g.14660186T>A , CM000674.1:g.14660186T>A GRCh37
NC_000012.10:g.14551453T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1187-134A>T MANE Select ENSP00000240617.5:n.1187-134A>T
ENST00000240617.9:c.1187-134A>T ENSP00000240617.5:n.1187-134A>T
NM_024829.5:c.1187-134A>T NP_079105.4:n.1187-134A>T
NM_024829.6:c.1187-134A>T MANE Select NP_079105.4:n.1187-134A>T