Canonical Allele Identifier: CA383982290
Gene: PLBD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14507104A>G , CM000674.2:g.14507104A>G GRCh38
NC_000012.11:g.14660038A>G , CM000674.1:g.14660038A>G GRCh37
NC_000012.10:g.14551305A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1201T>C MANE Select ENSP00000240617.5:p.Tyr401His
ENST00000240617.9:c.1201T>C ENSP00000240617.5:p.Tyr401His
NM_024829.5:c.1201T>C NP_079105.4:p.Tyr401His
NM_024829.6:c.1201T>C MANE Select NP_079105.4:p.Tyr401His