Canonical Allele Identifier: CA13827836
Gene: PLUT HGNC NCBI

Linked Data

ClinVar Variation Id: 669733
ClinVar RCV Id: RCV000828829
dbSNP Id: rs9581943
gnomAD v2: 13-28493997-G-A
gnomAD v3: 13-27919860-G-A
gnomAD v4: 13-27919860-G-A
MyVariant Identifiers: chr13:g.28493997G>A (hg19) chr13:g.27919860G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27919860G>A , CM000675.2:g.27919860G>A GRCh38
NC_000013.10:g.28493997G>A , CM000675.1:g.28493997G>A GRCh37
NC_000013.9:g.27391997G>A NCBI36
NG_008183.1:g.4830G>A

Transcript Alleles

HGVS Amino-acid change
NR_047484.1:n.241+1304C>T
Search 100 bp 5'
Search 100 bp 3'