Canonical Allele Identifier: CA1926080688
Gene: PAPSS2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727117A= , CM000672.2:g.87727117A= GRCh38
NC_000010.10:g.89486874A= , CM000672.1:g.89486874A= GRCh37
NC_000010.9:g.89476854A= NCBI36
NG_012150.1:g.72399A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-167A= MANE Select ENSP00000406157.1:n.881-167A=
ENST00000361175.8:c.866-167A= ENSP00000354436.4:n.866-167A=
ENST00000456849.1:c.881-167A= ENSP00000406157.1:n.881-167A=
NM_001015880.1:c.881-167A= NP_001015880.1:n.881-167A=
NM_004670.3:c.866-167A= NP_004661.2:n.866-167A=
NM_001015880.2:c.881-167A= MANE Select NP_001015880.1:n.881-167A=
NM_004670.4:c.866-167A= NP_004661.2:n.866-167A=
Search 100 bp 5'
Search 100 bp 3'