Canonical Allele Identifier: CA1586592326
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1581035877
gnomAD v4: 5-140113994-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140113994A>G , CM000667.2:g.140113994A>G GRCh38
NC_000005.9:g.139493579A>G , CM000667.1:g.139493579A>G GRCh37
NC_000005.8:g.139473763A>G NCBI36
NG_041813.1:g.4872A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-141-47A>G ENSP00000498560.1:n.-141-47A>G
ENST00000651386.1:c.-141-47A>G ENSP00000499133.1:n.-141-47A>G
ENST00000502351.1:n.283-47A>G
ENST00000505703.1:n.325-47A>G
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