Canonical Allele Identifier: CA2588336211
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI

Linked Data

gnomAD v4: 19-10223756-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223756C>A , CM000681.2:g.10223756C>A GRCh38
NC_000019.9:g.10334432C>A , CM000681.1:g.10334432C>A GRCh37
NC_000019.8:g.10195432C>A NCBI36
NG_028016.3:g.12531G>T , LRG_362:g.12531G>T
NG_046802.1:g.13052G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.*88G>T (S1PR2) MANE Select ENSP00000496438.1:n.*88G>T
ENST00000588952.5:c.-401-4887G>T (DNMT1) ENSP00000467050.1:n.-401-4887G>T
ENST00000590320.2:c.*88G>T (S1PR2) ENSP00000466933.1:n.*88G>T
ENST00000592342.5:c.-284+7448G>T (DNMT1) ENSP00000465993.1:n.-284+7448G>T
NM_004230.3:c.*88G>T (S1PR2) NP_004221.3:n.*88G>T
XM_011528425.1:c.894+256G>T (S1PR2) XP_011526727.1:n.894+256G>T
NM_004230.4:c.*88G>T (S1PR2) MANE Select NP_004221.3:n.*88G>T
Search 100 bp 5'
Search 100 bp 3'