Canonical Allele Identifier: CA10742615
Gene: MPC2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10489202

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167933841G>T , CM000663.2:g.167933841G>T GRCh38
NC_000001.10:g.167903079G>T , CM000663.1:g.167903079G>T GRCh37
NC_000001.9:g.166169703G>T NCBI36
NG_053062.1:g.2603G>T

Transcript Alleles

HGVS Amino-acid change
NM_001143674.3:c.109+1892C>A VV NP_001137146.1:p.=
NM_015415.3:c.109+1892C>A VV NP_056230.1:p.=
NR_026550.2:n.469+1892C>A
XM_006711266.2:c.109+1892C>A XP_006711329.1:p.=
XM_006711266.3:c.109+1892C>A
NM_001143674.4:c.109+1892C>A VV MANE Preferred
ENST00000271373.8:c.109+1892C>A ENSP00000271373.4:p.=
ENST00000367846.8:c.109+1892C>A ENSP00000356820.4:p.=
ENST00000458574.1:c.109+1892C>A ENSP00000392874.1:p.=