Canonical Allele Identifier: CA403944788

Gene: S1PR2 DNMT1

Linked Data

• dbSNP Id: rs1423289554
• gnomAD v2: 19-10334536-C-T
• gnomAD v4: 19-10223860-C-T
• MyVariant Identifiers: chr19:g.10334536C>T (hg19) ; chr19:g.10223860C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10223860C>T , CM000681.2:g.10223860C>T	GRCh38
NC_000019.9:g.10334536C>T , CM000681.1:g.10334536C>T	GRCh37
NC_000019.8:g.10195536C>T	NCBI36
NG_028016.3:g.12427G>A , LRG_362:g.12427G>A
NG_046802.1:g.12948G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646641.1:c.1046G>A (S1PR2) MANE Select	ENSP00000496438.1:p.Gly349Asp
ENST00000588952.5:c.-401-4991G>A (DNMT1)	ENSP00000467050.1:n.-401-4991G>A
ENST00000590320.2:c.1046G>A (S1PR2)	ENSP00000466933.1:p.Gly349Asp
ENST00000592342.5:c.-284+7344G>A (DNMT1)	ENSP00000465993.1:n.-284+7344G>A
NM_004230.3:c.1046G>A (S1PR2)	NP_004221.3:p.Gly349Asp
XM_011528425.1:c.894+152G>A (S1PR2)	XP_011526727.1:n.894+152G>A
NM_004230.4:c.1046G>A (S1PR2) MANE Select	NP_004221.3:p.Gly349Asp