Canonical Allele Identifier: CA383981912
Gene: PLBD1 HGNC NCBI

Linked Data

dbSNP Id: rs2136902923
MyVariant Identifiers: chr12:g.14659865A>G (hg19) chr12:g.14506931A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506931A>G , CM000674.2:g.14506931A>G GRCh38
NC_000012.11:g.14659865A>G , CM000674.1:g.14659865A>G GRCh37
NC_000012.10:g.14551132A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1372+2T>C MANE Select ENSP00000240617.5:n.1372+2T>C
ENST00000240617.9:c.1372+2T>C ENSP00000240617.5:n.1372+2T>C
NM_024829.5:c.1372+2T>C NP_079105.4:n.1372+2T>C
NM_024829.6:c.1372+2T>C MANE Select NP_079105.4:n.1372+2T>C
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