Canonical Allele Identifier: CA505467738

Gene: S1PR2 DNMT1

Linked Data

• dbSNP Id: rs1303223541
• gnomAD v2: 19-10334607-G-A
• gnomAD v4: 19-10223931-G-A
• MyVariant Identifiers: chr19:g.10334607G>A (hg19) ; chr19:g.10223931G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10223931G>A , CM000681.2:g.10223931G>A	GRCh38
NC_000019.9:g.10334607G>A , CM000681.1:g.10334607G>A	GRCh37
NC_000019.8:g.10195607G>A	NCBI36
NG_028016.3:g.12356C>T , LRG_362:g.12356C>T
NG_046802.1:g.12877C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646641.1:c.975C>T (S1PR2) MANE Select	ENSP00000496438.1:p.Leu325=
ENST00000588952.5:c.-401-5062C>T (DNMT1)	ENSP00000467050.1:n.-401-5062C>T
ENST00000590320.2:c.975C>T (S1PR2)	ENSP00000466933.1:p.Leu325=
ENST00000592342.5:c.-284+7273C>T (DNMT1)	ENSP00000465993.1:n.-284+7273C>T
NM_004230.3:c.975C>T (S1PR2)	NP_004221.3:p.Leu325=
XM_011528425.1:c.894+81C>T (S1PR2)	XP_011526727.1:n.894+81C>T
NM_004230.4:c.975C>T (S1PR2) MANE Select	NP_004221.3:p.Leu325=