Canonical Allele Identifier: CA1008868866

Gene: MPC2

Linked Data

• gnomAD v3: 1-167933820-T-C
• gnomAD v4: 1-167933820-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167933820T>C , CM000663.2:g.167933820T>C	GRCh38
NC_000001.10:g.167903058T>C , CM000663.1:g.167903058T>C	GRCh37
NC_000001.9:g.166169682T>C	NCBI36
NG_053062.1:g.2582T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271373.9:c.109+1913A>G MANE Select	ENSP00000271373.4:n.109+1913A>G
ENST00000271373.8:c.109+1913A>G	ENSP00000271373.4:n.109+1913A>G
ENST00000367846.8:c.109+1913A>G	ENSP00000356820.4:n.109+1913A>G
ENST00000458574.1:c.109+1913A>G	ENSP00000392874.1:n.109+1913A>G
NM_001143674.3:c.109+1913A>G	NP_001137146.1:n.109+1913A>G
NM_015415.3:c.109+1913A>G	NP_056230.1:n.109+1913A>G
NR_026550.2:n.469+1913A>G
XM_006711266.2:c.109+1913A>G	XP_006711329.1:n.109+1913A>G
XM_006711266.3:c.109+1913A>G	XP_006711329.1:n.109+1913A>G
NM_001143674.4:c.109+1913A>G MANE Select	NP_001137146.1:n.109+1913A>G
NR_026550.3:n.264+1913A>G