Canonical Allele Identifier: CA403944963
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10334558T>G (hg19) chr19:g.10223882T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10223882T>G , CM000681.2:g.10223882T>G GRCh38
NC_000019.9:g.10334558T>G , CM000681.1:g.10334558T>G GRCh37
NC_000019.8:g.10195558T>G NCBI36
NG_028016.3:g.12405A>C , LRG_362:g.12405A>C
NG_046802.1:g.12926A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.1024A>C (S1PR2) MANE Select ENSP00000496438.1:p.Thr342Pro
ENST00000588952.5:c.-401-5013A>C (DNMT1) ENSP00000467050.1:n.-401-5013A>C
ENST00000590320.2:c.1024A>C (S1PR2) ENSP00000466933.1:p.Thr342Pro
ENST00000592342.5:c.-284+7322A>C (DNMT1) ENSP00000465993.1:n.-284+7322A>C
NM_004230.3:c.1024A>C (S1PR2) NP_004221.3:p.Thr342Pro
XM_011528425.1:c.894+130A>C (S1PR2) XP_011526727.1:n.894+130A>C
NM_004230.4:c.1024A>C (S1PR2) MANE Select NP_004221.3:p.Thr342Pro
Search 100 bp 5'
Search 100 bp 3'