Canonical Allele Identifier: CA377489295
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89487053A>C (hg19) chr10:g.87727296A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727296A>C , CM000672.2:g.87727296A>C GRCh38
NC_000010.10:g.89487053A>C , CM000672.1:g.89487053A>C GRCh37
NC_000010.9:g.89477033A>C NCBI36
NG_012150.1:g.72578A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.893A>C MANE Select ENSP00000406157.1:p.Asn298Thr
ENST00000361175.8:c.878A>C ENSP00000354436.4:p.Asn293Thr
ENST00000456849.1:c.893A>C ENSP00000406157.1:p.Asn298Thr
NM_001015880.1:c.893A>C NP_001015880.1:p.Asn298Thr
NM_004670.3:c.878A>C NP_004661.2:p.Asn293Thr
NM_001015880.2:c.893A>C MANE Select NP_001015880.1:p.Asn298Thr
NM_004670.4:c.878A>C NP_004661.2:p.Asn293Thr
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