Canonical Allele Identifier: CA804698494
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1183756669
gnomAD v3: 5-140114080-G-A
gnomAD v4: 5-140114080-G-A
MyVariant Identifiers: chr5:g.139493665G>A (hg19) chr5:g.140114080G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114080G>A , CM000667.2:g.140114080G>A GRCh38
NC_000005.9:g.139493665G>A , CM000667.1:g.139493665G>A GRCh37
NC_000005.8:g.139473849G>A NCBI36
NG_041813.1:g.4958G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-102G>A ENSP00000498560.1:n.-102G>A
ENST00000651386.1:c.-102G>A ENSP00000499133.1:n.-102G>A
ENST00000502351.1:n.322G>A
ENST00000505703.1:n.364G>A
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