Canonical Allele Identifier: CA342782
Gene: POLR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 31148
ClinVar RCV Id: RCV000024144
dbSNP Id: rs267608681
MyVariant Identifiers: chr10:g.79753052A>T (hg19) chr10:g.77993294A>T (hg38)
PubMed: PMID:22036171 PMID:22855961
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77993294A>T , CM000672.2:g.77993294A>T GRCh38
NC_000010.10:g.79753052A>T , CM000672.1:g.79753052A>T GRCh37
NC_000010.9:g.79423058A>T NCBI36
NG_029648.1:g.41247T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698727.1:n.1750T>A
ENST00000698728.1:n.2269T>A
ENST00000698729.1:n.3815T>A
ENST00000698730.1:n.3815T>A
ENST00000698731.1:c.2549T>A ENSP00000513898.1:p.Ile850Asn
ENST00000698732.1:c.*1551T>A ENSP00000513899.1:n.*1551T>A
ENST00000698733.1:c.*1877T>A ENSP00000513900.1:n.*1877T>A
ENST00000698734.1:c.*214T>A ENSP00000513901.1:n.*214T>A
ENST00000698735.1:n.2805T>A
ENST00000698736.1:n.2805T>A
ENST00000698737.1:n.2805T>A
ENST00000698738.1:n.2805T>A
ENST00000698739.1:n.2805T>A
ENST00000372371.8:c.2690T>A MANE Select ENSP00000361446.3:p.Ile897Asn
ENST00000372371.7:c.2690T>A ENSP00000361446.3:p.Ile897Asn
ENST00000472014.5:n.543T>A
NM_007055.3:c.2690T>A NP_008986.2:p.Ile897Asn
NM_007055.4:c.2690T>A MANE Select NP_008986.2:p.Ile897Asn
Search 100 bp 5'
Search 100 bp 3'