Canonical Allele Identifier: CA14690152
Gene: PLAUR HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.43670289C>T
GRCh37 chr19:g.44174441C>T
gnomAD v2:
19:44174441 C / T
gnomAD v3:
19:43670289 C / T
gnomAD v4:
chr19-43670289-C-T
Joint Max Group AF 0.06819632 (AFR)
Genomes Max Group AF 0.06729861 (AFR)
Exomes Max Group AF 0.06841672 (AFR)
dbSNP:
4251805
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43670289C>T , CM000681.2:g.43670289C>T GRCh38
NC_000019.9:g.44174441C>T , CM000681.1:g.44174441C>T GRCh37
NC_000019.8:g.48866281C>T NCBI36
NG_032898.1:g.5058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221264.8:c.-169G>A ENSP00000221264.3:n.-169G>A
ENST00000340093.7:c.-169G>A ENSP00000339328.3:n.-169G>A
NM_001005376.2:c.-169G>A NP_001005376.1:n.-169G>A
NM_001005377.2:c.-169G>A NP_001005377.1:n.-169G>A
NM_001301037.1:c.-169G>A NP_001287966.1:n.-169G>A
NM_002659.3:c.-169G>A NP_002650.1:n.-169G>A
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