Canonical Allele Identifier: CA2610038235
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs2131720538
gnomAD v4: 10-87727238-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727238C>T , CM000672.2:g.87727238C>T GRCh38
NC_000010.10:g.89486995C>T , CM000672.1:g.89486995C>T GRCh37
NC_000010.9:g.89476975C>T NCBI36
NG_012150.1:g.72520C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-46C>T MANE Select ENSP00000406157.1:n.881-46C>T
ENST00000361175.8:c.866-46C>T ENSP00000354436.4:n.866-46C>T
ENST00000456849.1:c.881-46C>T ENSP00000406157.1:n.881-46C>T
NM_001015880.1:c.881-46C>T NP_001015880.1:n.881-46C>T
NM_004670.3:c.866-46C>T NP_004661.2:n.866-46C>T
NM_001015880.2:c.881-46C>T MANE Select NP_001015880.1:n.881-46C>T
NM_004670.4:c.866-46C>T NP_004661.2:n.866-46C>T
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