Canonical Allele Identifier: CA804698499
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1197298012
gnomAD v3: 5-140114097-G-C
gnomAD v4: 5-140114097-G-C
MyVariant Identifiers: chr5:g.139493682G>C (hg19) chr5:g.140114097G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114097G>C , CM000667.2:g.140114097G>C GRCh38
NC_000005.9:g.139493682G>C , CM000667.1:g.139493682G>C GRCh37
NC_000005.8:g.139473866G>C NCBI36
NG_041813.1:g.4975G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-85G>C ENSP00000498560.1:n.-85G>C
ENST00000651386.1:c.-85G>C ENSP00000499133.1:n.-85G>C
ENST00000502351.1:n.339G>C
ENST00000505703.1:n.381G>C
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