Canonical Allele Identifier: CA804698492
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1244481801
gnomAD v4: 5-140114071-G-A
MyVariant Identifiers: chr5:g.139493656G>A (hg19) chr5:g.140114071G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114071G>A , CM000667.2:g.140114071G>A GRCh38
NC_000005.9:g.139493656G>A , CM000667.1:g.139493656G>A GRCh37
NC_000005.8:g.139473840G>A NCBI36
NG_041813.1:g.4949G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-111G>A ENSP00000498560.1:n.-111G>A
ENST00000651386.1:c.-111G>A ENSP00000499133.1:n.-111G>A
ENST00000502351.1:n.313G>A
ENST00000505703.1:n.355G>A
Search 100 bp 5'
Search 100 bp 3'