Canonical Allele Identifier: CA783165946

Gene: S1PR2 DNMT1

Linked Data

• dbSNP Id: rs1346503694
• gnomAD v3: 19-10223768-G-A
• gnomAD v4: 19-10223768-G-A
• MyVariant Identifiers: chr19:g.10334444G>A (hg19) ; chr19:g.10223768G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10223768G>A , CM000681.2:g.10223768G>A	GRCh38
NC_000019.9:g.10334444G>A , CM000681.1:g.10334444G>A	GRCh37
NC_000019.8:g.10195444G>A	NCBI36
NG_028016.3:g.12519C>T , LRG_362:g.12519C>T
NG_046802.1:g.13040C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646641.1:c.*76C>T (S1PR2) MANE Select	ENSP00000496438.1:n.*76C>T
ENST00000588952.5:c.-401-4899C>T (DNMT1)	ENSP00000467050.1:n.-401-4899C>T
ENST00000590320.2:c.*76C>T (S1PR2)	ENSP00000466933.1:n.*76C>T
ENST00000592342.5:c.-284+7436C>T (DNMT1)	ENSP00000465993.1:n.-284+7436C>T
NM_004230.3:c.*76C>T (S1PR2)	NP_004221.3:n.*76C>T
XM_011528425.1:c.894+244C>T (S1PR2)	XP_011526727.1:n.894+244C>T
NM_004230.4:c.*76C>T (S1PR2) MANE Select	NP_004221.3:n.*76C>T