Canonical Allele Identifier: CA2322323100
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223870A= , CM000681.2:g.10223870A= GRCh38
NC_000019.9:g.10334546A= , CM000681.1:g.10334546A= GRCh37
NC_000019.8:g.10195546A= NCBI36
NG_028016.3:g.12417T= , LRG_362:g.12417T=
NG_046802.1:g.12938T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.1036T= (S1PR2) MANE Select ENSP00000496438.1:p.Phe346=
ENST00000588952.5:c.-401-5001T= (DNMT1) ENSP00000467050.1:n.-401-5001T=
ENST00000590320.2:c.1036T= (S1PR2) ENSP00000466933.1:p.Phe346=
ENST00000592342.5:c.-284+7334T= (DNMT1) ENSP00000465993.1:n.-284+7334T=
NM_004230.3:c.1036T= (S1PR2) NP_004221.3:p.Phe346=
XM_011528425.1:c.894+142T= (S1PR2) XP_011526727.1:n.894+142T=
NM_004230.4:c.1036T= (S1PR2) MANE Select NP_004221.3:p.Phe346=
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