Canonical Allele Identifier: CA1205465745

Gene: MPC2

Linked Data

• dbSNP Id: rs1670982898

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167933801C>T , CM000663.2:g.167933801C>T	GRCh38
NC_000001.10:g.167903039C>T , CM000663.1:g.167903039C>T	GRCh37
NC_000001.9:g.166169663C>T	NCBI36
NG_053062.1:g.2563C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271373.9:c.109+1932G>A MANE Select	ENSP00000271373.4:n.109+1932G>A
ENST00000271373.8:c.109+1932G>A	ENSP00000271373.4:n.109+1932G>A
ENST00000367846.8:c.109+1932G>A	ENSP00000356820.4:n.109+1932G>A
ENST00000458574.1:c.109+1932G>A	ENSP00000392874.1:n.109+1932G>A
NM_001143674.3:c.109+1932G>A	NP_001137146.1:n.109+1932G>A
NM_015415.3:c.109+1932G>A	NP_056230.1:n.109+1932G>A
NR_026550.2:n.469+1932G>A
XM_006711266.2:c.109+1932G>A	XP_006711329.1:n.109+1932G>A
XM_006711266.3:c.109+1932G>A	XP_006711329.1:n.109+1932G>A
NM_001143674.4:c.109+1932G>A MANE Select	NP_001137146.1:n.109+1932G>A
NR_026550.3:n.264+1932G>A