Canonical Allele Identifier: CA804698525
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs188901068
MyVariant Identifiers: chr5:g.139493700G>C (hg19) chr5:g.140114115G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114115G>C , CM000667.2:g.140114115G>C GRCh38
NC_000005.9:g.139493700G>C , CM000667.1:g.139493700G>C GRCh37
NC_000005.8:g.139473884G>C NCBI36
NG_041813.1:g.4993G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-67G>C MANE Select ENSP00000332706.3:n.-67G>C
ENST00000505703.2:c.-67G>C ENSP00000498560.1:n.-67G>C
ENST00000651386.1:c.-67G>C ENSP00000499133.1:n.-67G>C
ENST00000502351.1:n.357G>C
ENST00000505703.1:n.399G>C
NM_005859.5:c.-67G>C MANE Select NP_005850.1:n.-67G>C
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