Canonical Allele Identifier: CA804698428
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1261035464
gnomAD v4: 5-140114006-G-T
MyVariant Identifiers: chr5:g.139493591G>T (hg19) chr5:g.140114006G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114006G>T , CM000667.2:g.140114006G>T GRCh38
NC_000005.9:g.139493591G>T , CM000667.1:g.139493591G>T GRCh37
NC_000005.8:g.139473775G>T NCBI36
NG_041813.1:g.4884G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-141-35G>T ENSP00000498560.1:n.-141-35G>T
ENST00000651386.1:c.-141-35G>T ENSP00000499133.1:n.-141-35G>T
ENST00000502351.1:n.283-35G>T
ENST00000505703.1:n.325-35G>T
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