Canonical Allele Identifier: CA2576616817
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI

Linked Data

gnomAD v4: 19-10223780-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223780G>T , CM000681.2:g.10223780G>T GRCh38
NC_000019.9:g.10334456G>T , CM000681.1:g.10334456G>T GRCh37
NC_000019.8:g.10195456G>T NCBI36
NG_028016.3:g.12507C>A , LRG_362:g.12507C>A
NG_046802.1:g.13028C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.*64C>A (S1PR2) MANE Select ENSP00000496438.1:n.*64C>A
ENST00000588952.5:c.-401-4911C>A (DNMT1) ENSP00000467050.1:n.-401-4911C>A
ENST00000590320.2:c.*64C>A (S1PR2) ENSP00000466933.1:n.*64C>A
ENST00000592342.5:c.-284+7424C>A (DNMT1) ENSP00000465993.1:n.-284+7424C>A
NM_004230.3:c.*64C>A (S1PR2) NP_004221.3:n.*64C>A
XM_011528425.1:c.894+232C>A (S1PR2) XP_011526727.1:n.894+232C>A
NM_004230.4:c.*64C>A (S1PR2) MANE Select NP_004221.3:n.*64C>A
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