Canonical Allele Identifier: CA2602580564
Gene: PDSS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107245678T>A , CM000668.2:g.107245678T>A GRCh38
NC_000006.11:g.107566882T>A , CM000668.1:g.107566882T>A GRCh37
NC_000006.10:g.107673575T>A NCBI36
NG_013033.1:g.218898A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369037.9:c.631-59A>T MANE Select ENSP00000358033.4:n.631-59A>T
ENST00000369037.8:c.631-59A>T ENSP00000358033.4:n.631-59A>T
NM_020381.3:c.631-59A>T NP_065114.3:n.631-59A>T
XM_011535956.1:c.631-59A>T XP_011534258.1:n.631-59A>T
XM_011535957.1:c.631-59A>T XP_011534259.1:n.631-59A>T
XM_011535958.1:c.496-59A>T XP_011534260.1:n.496-59A>T
XM_011535959.1:c.631-59A>T XP_011534261.1:n.631-59A>T
XM_011535960.1:c.223-59A>T XP_011534262.1:n.223-59A>T
XM_011535961.1:c.631-59A>T XP_011534263.1:n.631-59A>T
XM_011535962.1:c.223-59A>T XP_011534264.1:n.223-59A>T
XM_011535956.3:c.631-59A>T XP_011534258.1:n.631-59A>T
XM_011535957.3:c.631-59A>T XP_011534259.1:n.631-59A>T
XM_011535958.3:c.496-59A>T XP_011534260.1:n.496-59A>T
XM_011535959.3:c.631-59A>T XP_011534261.1:n.631-59A>T
XM_011535960.3:c.223-59A>T XP_011534262.1:n.223-59A>T
XM_011535961.3:c.631-59A>T XP_011534263.1:n.631-59A>T
XM_011535962.2:c.223-59A>T XP_011534264.1:n.223-59A>T
XM_017011082.2:c.631-59A>T XP_016866571.1:n.631-59A>T
NM_020381.4:c.631-59A>T MANE Select NP_065114.3:n.631-59A>T