Canonical Allele Identifier: CA1926080682
Gene: PAPSS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727100C= , CM000672.2:g.87727100C= GRCh38
NC_000010.10:g.89486857C= , CM000672.1:g.89486857C= GRCh37
NC_000010.9:g.89476837C= NCBI36
NG_012150.1:g.72382C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-184C= MANE Select ENSP00000406157.1:n.881-184C=
ENST00000361175.8:c.866-184C= ENSP00000354436.4:n.866-184C=
ENST00000456849.1:c.881-184C= ENSP00000406157.1:n.881-184C=
NM_001015880.1:c.881-184C= NP_001015880.1:n.881-184C=
NM_004670.3:c.866-184C= NP_004661.2:n.866-184C=
NM_001015880.2:c.881-184C= MANE Select NP_001015880.1:n.881-184C=
NM_004670.4:c.866-184C= NP_004661.2:n.866-184C=
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