Canonical Allele Identifier: CA451564347
Gene: PDSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.107566809T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107245605T>C , CM000668.2:g.107245605T>C GRCh38
NC_000006.11:g.107566809T>C , CM000668.1:g.107566809T>C GRCh37
NC_000006.10:g.107673502T>C NCBI36
NG_013033.1:g.218971A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369037.9:c.645A>G MANE Select ENSP00000358033.4:p.Leu215=
ENST00000369037.8:c.645A>G ENSP00000358033.4:p.Leu215=
NM_020381.3:c.645A>G NP_065114.3:p.Leu215=
XM_011535956.1:c.645A>G XP_011534258.1:p.Leu215=
XM_011535957.1:c.645A>G XP_011534259.1:p.Leu215=
XM_011535958.1:c.510A>G XP_011534260.1:p.Leu170=
XM_011535959.1:c.645A>G XP_011534261.1:p.Leu215=
XM_011535960.1:c.237A>G XP_011534262.1:p.Leu79=
XM_011535961.1:c.645A>G XP_011534263.1:p.Leu215=
XM_011535962.1:c.237A>G XP_011534264.1:p.Leu79=
XM_011535956.3:c.645A>G XP_011534258.1:p.Leu215=
XM_011535957.3:c.645A>G XP_011534259.1:p.Leu215=
XM_011535958.3:c.510A>G XP_011534260.1:p.Leu170=
XM_011535959.3:c.645A>G XP_011534261.1:p.Leu215=
XM_011535960.3:c.237A>G XP_011534262.1:p.Leu79=
XM_011535961.3:c.645A>G XP_011534263.1:p.Leu215=
XM_011535962.2:c.237A>G XP_011534264.1:p.Leu79=
XM_017011082.2:c.645A>G XP_016866571.1:p.Leu215=
NM_020381.4:c.645A>G MANE Select NP_065114.3:p.Leu215=