Canonical Allele Identifier: CA365323025
Gene: PDSS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107245553A>C , CM000668.2:g.107245553A>C GRCh38
NC_000006.11:g.107566757A>C , CM000668.1:g.107566757A>C GRCh37
NC_000006.10:g.107673450A>C NCBI36
NG_013033.1:g.219023T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369037.9:c.697T>G MANE Select ENSP00000358033.4:p.Ser233Ala
ENST00000369037.8:c.697T>G ENSP00000358033.4:p.Ser233Ala
NM_020381.3:c.697T>G NP_065114.3:p.Ser233Ala
XM_011535956.1:c.697T>G XP_011534258.1:p.Ser233Ala
XM_011535957.1:c.697T>G XP_011534259.1:p.Ser233Ala
XM_011535958.1:c.562T>G XP_011534260.1:p.Ser188Ala
XM_011535959.1:c.697T>G XP_011534261.1:p.Ser233Ala
XM_011535960.1:c.289T>G XP_011534262.1:p.Ser97Ala
XM_011535961.1:c.697T>G XP_011534263.1:p.Ser233Ala
XM_011535962.1:c.289T>G XP_011534264.1:p.Ser97Ala
XM_011535956.3:c.697T>G XP_011534258.1:p.Ser233Ala
XM_011535957.3:c.697T>G XP_011534259.1:p.Ser233Ala
XM_011535958.3:c.562T>G XP_011534260.1:p.Ser188Ala
XM_011535959.3:c.697T>G XP_011534261.1:p.Ser233Ala
XM_011535960.3:c.289T>G XP_011534262.1:p.Ser97Ala
XM_011535961.3:c.697T>G XP_011534263.1:p.Ser233Ala
XM_011535962.2:c.289T>G XP_011534264.1:p.Ser97Ala
XM_017011082.2:c.697T>G XP_016866571.1:p.Ser233Ala
NM_020381.4:c.697T>G MANE Select NP_065114.3:p.Ser233Ala