Canonical Allele Identifier: CA1926080698
Gene: PAPSS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727138G= , CM000672.2:g.87727138G= GRCh38
NC_000010.10:g.89486895G= , CM000672.1:g.89486895G= GRCh37
NC_000010.9:g.89476875G= NCBI36
NG_012150.1:g.72420G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-146G= MANE Select ENSP00000406157.1:n.881-146G=
ENST00000361175.8:c.866-146G= ENSP00000354436.4:n.866-146G=
ENST00000456849.1:c.881-146G= ENSP00000406157.1:n.881-146G=
NM_001015880.1:c.881-146G= NP_001015880.1:n.881-146G=
NM_004670.3:c.866-146G= NP_004661.2:n.866-146G=
NM_001015880.2:c.881-146G= MANE Select NP_001015880.1:n.881-146G=
NM_004670.4:c.866-146G= NP_004661.2:n.866-146G=
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