Canonical Allele Identifier: CA2322323069
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223794C= , CM000681.2:g.10223794C= GRCh38
NC_000019.9:g.10334470C= , CM000681.1:g.10334470C= GRCh37
NC_000019.8:g.10195470C= NCBI36
NG_028016.3:g.12493G= , LRG_362:g.12493G=
NG_046802.1:g.13014G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.*50G= (S1PR2) MANE Select ENSP00000496438.1:n.*50G=
ENST00000588952.5:c.-401-4925G= (DNMT1) ENSP00000467050.1:n.-401-4925G=
ENST00000590320.2:c.*50G= (S1PR2) ENSP00000466933.1:n.*50G=
ENST00000592342.5:c.-284+7410G= (DNMT1) ENSP00000465993.1:n.-284+7410G=
NM_004230.3:c.*50G= (S1PR2) NP_004221.3:n.*50G=
XM_011528425.1:c.894+218G= (S1PR2) XP_011526727.1:n.894+218G=
NM_004230.4:c.*50G= (S1PR2) MANE Select NP_004221.3:n.*50G=
Search 100 bp 5'
Search 100 bp 3'