Canonical Allele Identifier: CA2610038229
Gene: PAPSS2 HGNC NCBI

Linked Data

gnomAD v4: 10-87727225-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727225G>C , CM000672.2:g.87727225G>C GRCh38
NC_000010.10:g.89486982G>C , CM000672.1:g.89486982G>C GRCh37
NC_000010.9:g.89476962G>C NCBI36
NG_012150.1:g.72507G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-59G>C MANE Select ENSP00000406157.1:n.881-59G>C
ENST00000361175.8:c.866-59G>C ENSP00000354436.4:n.866-59G>C
ENST00000456849.1:c.881-59G>C ENSP00000406157.1:n.881-59G>C
NM_001015880.1:c.881-59G>C NP_001015880.1:n.881-59G>C
NM_004670.3:c.866-59G>C NP_004661.2:n.866-59G>C
NM_001015880.2:c.881-59G>C MANE Select NP_001015880.1:n.881-59G>C
NM_004670.4:c.866-59G>C NP_004661.2:n.866-59G>C
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