Canonical Allele Identifier: CA2322323085
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223840A= , CM000681.2:g.10223840A= GRCh38
NC_000019.9:g.10334516A= , CM000681.1:g.10334516A= GRCh37
NC_000019.8:g.10195516A= NCBI36
NG_028016.3:g.12447T= , LRG_362:g.12447T=
NG_046802.1:g.12968T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.*4T= (S1PR2) MANE Select ENSP00000496438.1:n.*4T=
ENST00000588952.5:c.-401-4971T= (DNMT1) ENSP00000467050.1:n.-401-4971T=
ENST00000590320.2:c.*4T= (S1PR2) ENSP00000466933.1:n.*4T=
ENST00000592342.5:c.-284+7364T= (DNMT1) ENSP00000465993.1:n.-284+7364T=
NM_004230.3:c.*4T= (S1PR2) NP_004221.3:n.*4T=
XM_011528425.1:c.894+172T= (S1PR2) XP_011526727.1:n.894+172T=
NM_004230.4:c.*4T= (S1PR2) MANE Select NP_004221.3:n.*4T=
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