Canonical Allele Identifier: CA5589589
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs778792401
ExAC: 10:89486999 C / A
gnomAD v2: 10-89486999-C-A
gnomAD v3: 10-87727242-C-A
gnomAD v4: 10-87727242-C-A
MyVariant Identifiers: chr10:g.89486999C>A (hg19) chr10:g.87727242C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727242C>A , CM000672.2:g.87727242C>A GRCh38
NC_000010.10:g.89486999C>A , CM000672.1:g.89486999C>A GRCh37
NC_000010.9:g.89476979C>A NCBI36
NG_012150.1:g.72524C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-42C>A MANE Select ENSP00000406157.1:n.881-42C>A
ENST00000361175.8:c.866-42C>A ENSP00000354436.4:n.866-42C>A
ENST00000456849.1:c.881-42C>A ENSP00000406157.1:n.881-42C>A
NM_001015880.1:c.881-42C>A NP_001015880.1:n.881-42C>A
NM_004670.3:c.866-42C>A NP_004661.2:n.866-42C>A
NM_001015880.2:c.881-42C>A MANE Select NP_001015880.1:n.881-42C>A
NM_004670.4:c.866-42C>A NP_004661.2:n.866-42C>A
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