Canonical Allele Identifier: CA2675565032
Gene: PURA HGNC NCBI

Linked Data

gnomAD v4: 5-140113982-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140113982A>T , CM000667.2:g.140113982A>T GRCh38
NC_000005.9:g.139493567A>T , CM000667.1:g.139493567A>T GRCh37
NC_000005.8:g.139473751A>T NCBI36
NG_041813.1:g.4860A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-141-59A>T ENSP00000498560.1:n.-141-59A>T
ENST00000651386.1:c.-141-59A>T ENSP00000499133.1:n.-141-59A>T
ENST00000502351.1:n.283-59A>T
ENST00000505703.1:n.325-59A>T
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