Canonical Allele Identifier: CA563504632
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1159823451
gnomAD v2: 5-139493568-C-T
gnomAD v3: 5-140113983-C-T
gnomAD v4: 5-140113983-C-T
MyVariant Identifiers: chr5:g.139493568C>T (hg19) chr5:g.140113983C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140113983C>T , CM000667.2:g.140113983C>T GRCh38
NC_000005.9:g.139493568C>T , CM000667.1:g.139493568C>T GRCh37
NC_000005.8:g.139473752C>T NCBI36
NG_041813.1:g.4861C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-141-58C>T ENSP00000498560.1:n.-141-58C>T
ENST00000651386.1:c.-141-58C>T ENSP00000499133.1:n.-141-58C>T
ENST00000502351.1:n.283-58C>T
ENST00000505703.1:n.325-58C>T
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