Canonical Allele Identifier: CA403947826
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI

Linked Data

gnomAD v4: 19-10224413-G-T
MyVariant Identifiers: chr19:g.10335089G>T (hg19) chr19:g.10224413G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10224413G>T , CM000681.2:g.10224413G>T GRCh38
NC_000019.9:g.10335089G>T , CM000681.1:g.10335089G>T GRCh37
NC_000019.8:g.10196089G>T NCBI36
NG_028016.3:g.11874C>A , LRG_362:g.11874C>A
NG_046802.1:g.12395C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646641.1:c.493C>A (S1PR2) MANE Select ENSP00000496438.1:p.Leu165Met
ENST00000588952.5:c.-401-5544C>A (DNMT1) ENSP00000467050.1:n.-401-5544C>A
ENST00000590320.2:c.493C>A (S1PR2) ENSP00000466933.1:p.Leu165Met
ENST00000592342.5:c.-284+6791C>A (DNMT1) ENSP00000465993.1:n.-284+6791C>A
NM_004230.3:c.493C>A (S1PR2) NP_004221.3:p.Leu165Met
XM_011528425.1:c.493C>A (S1PR2) XP_011526727.1:p.Leu165Met
NM_004230.4:c.493C>A (S1PR2) MANE Select NP_004221.3:p.Leu165Met
Search 100 bp 5'
Search 100 bp 3'