Canonical Allele Identifier: CA1586592419
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1763030031

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114041A>G , CM000667.2:g.140114041A>G GRCh38
NC_000005.9:g.139493626A>G , CM000667.1:g.139493626A>G GRCh37
NC_000005.8:g.139473810A>G NCBI36
NG_041813.1:g.4919A>G

Transcript Alleles

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