Canonical Allele Identifier: CA9188943
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 506084
ClinVar RCV Id: RCV000606394 RCV000713493 RCV003927954
dbSNP Id: rs116191851
ExAC: 19:10334532 G / A
gnomAD v2: 19-10334532-G-A
gnomAD v3: 19-10223856-G-A
gnomAD v4: 19-10223856-G-A
MyVariant Identifiers: chr19:g.10334532G>A (hg19) chr19:g.10223856G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223856G>A , CM000681.2:g.10223856G>A GRCh38
NC_000019.9:g.10334532G>A , CM000681.1:g.10334532G>A GRCh37
NC_000019.8:g.10195532G>A NCBI36
NG_028016.3:g.12431C>T , LRG_362:g.12431C>T
NG_046802.1:g.12952C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646641.1:c.1050C>T (S1PR2) MANE Select ENSP00000496438.1:p.Asn350=
ENST00000588952.5:c.-401-4987C>T (DNMT1) ENSP00000467050.1:n.-401-4987C>T
ENST00000590320.2:c.1050C>T (S1PR2) ENSP00000466933.1:p.Asn350=
ENST00000592342.5:c.-284+7348C>T (DNMT1) ENSP00000465993.1:n.-284+7348C>T
NM_004230.3:c.1050C>T (S1PR2) NP_004221.3:p.Asn350=
XM_011528425.1:c.894+156C>T (S1PR2) XP_011526727.1:n.894+156C>T
NM_004230.4:c.1050C>T (S1PR2) MANE Select NP_004221.3:p.Asn350=
Search 100 bp 5'
Search 100 bp 3'