Canonical Allele Identifier: CA1008868895
Gene: MPC2 HGNC NCBI

Linked Data

dbSNP Id: rs1670983614

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167933829T>A , CM000663.2:g.167933829T>A GRCh38
NC_000001.10:g.167903067T>A , CM000663.1:g.167903067T>A GRCh37
NC_000001.9:g.166169691T>A NCBI36
NG_053062.1:g.2591T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000271373.9:c.109+1904A>T MANE Select ENSP00000271373.4:n.109+1904A>T
ENST00000271373.8:c.109+1904A>T ENSP00000271373.4:n.109+1904A>T
ENST00000367846.8:c.109+1904A>T ENSP00000356820.4:n.109+1904A>T
ENST00000458574.1:c.109+1904A>T ENSP00000392874.1:n.109+1904A>T
NM_001143674.3:c.109+1904A>T NP_001137146.1:n.109+1904A>T
NM_015415.3:c.109+1904A>T NP_056230.1:n.109+1904A>T
NR_026550.2:n.469+1904A>T
XM_006711266.2:c.109+1904A>T XP_006711329.1:n.109+1904A>T
XM_006711266.3:c.109+1904A>T XP_006711329.1:n.109+1904A>T
NM_001143674.4:c.109+1904A>T MANE Select NP_001137146.1:n.109+1904A>T
NR_026550.3:n.264+1904A>T