Canonical Allele Identifier: CA403947225
Gene: S1PR2 HGNC NCBI
DNMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10334991G>C (hg19) chr19:g.10224315G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10224315G>C , CM000681.2:g.10224315G>C GRCh38
NC_000019.9:g.10334991G>C , CM000681.1:g.10334991G>C GRCh37
NC_000019.8:g.10195991G>C NCBI36
NG_028016.3:g.11972C>G , LRG_362:g.11972C>G
NG_046802.1:g.12493C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646641.1:c.591C>G (S1PR2) MANE Select ENSP00000496438.1:p.Ile197Met
ENST00000588952.5:c.-401-5446C>G (DNMT1) ENSP00000467050.1:n.-401-5446C>G
ENST00000590320.2:c.591C>G (S1PR2) ENSP00000466933.1:p.Ile197Met
ENST00000592342.5:c.-284+6889C>G (DNMT1) ENSP00000465993.1:n.-284+6889C>G
NM_004230.3:c.591C>G (S1PR2) NP_004221.3:p.Ile197Met
XM_011528425.1:c.591C>G (S1PR2) XP_011526727.1:p.Ile197Met
NM_004230.4:c.591C>G (S1PR2) MANE Select NP_004221.3:p.Ile197Met
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