Canonical Allele Identifier: CA1926080710
Gene: PAPSS2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727176G= , CM000672.2:g.87727176G= GRCh38
NC_000010.10:g.89486933G= , CM000672.1:g.89486933G= GRCh37
NC_000010.9:g.89476913G= NCBI36
NG_012150.1:g.72458G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-108G= MANE Select ENSP00000406157.1:n.881-108G=
ENST00000361175.8:c.866-108G= ENSP00000354436.4:n.866-108G=
ENST00000456849.1:c.881-108G= ENSP00000406157.1:n.881-108G=
NM_001015880.1:c.881-108G= NP_001015880.1:n.881-108G=
NM_004670.3:c.866-108G= NP_004661.2:n.866-108G=
NM_001015880.2:c.881-108G= MANE Select NP_001015880.1:n.881-108G=
NM_004670.4:c.866-108G= NP_004661.2:n.866-108G=
Search 100 bp 5'
Search 100 bp 3'