Canonical Allele Identifier: CA31413204

Gene: MPC2

Linked Data

• dbSNP Id: rs768101658
• MyVariant Identifiers: chr1:g.167903048A>G (hg19) ; chr1:g.167933810A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167933810A>G , CM000663.2:g.167933810A>G	GRCh38
NC_000001.10:g.167903048A>G , CM000663.1:g.167903048A>G	GRCh37
NC_000001.9:g.166169672A>G	NCBI36
NG_053062.1:g.2572A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271373.9:c.109+1923T>C MANE Select	ENSP00000271373.4:n.109+1923T>C
ENST00000271373.8:c.109+1923T>C	ENSP00000271373.4:n.109+1923T>C
ENST00000367846.8:c.109+1923T>C	ENSP00000356820.4:n.109+1923T>C
ENST00000458574.1:c.109+1923T>C	ENSP00000392874.1:n.109+1923T>C
NM_001143674.3:c.109+1923T>C	NP_001137146.1:n.109+1923T>C
NM_015415.3:c.109+1923T>C	NP_056230.1:n.109+1923T>C
NR_026550.2:n.469+1923T>C
XM_006711266.2:c.109+1923T>C	XP_006711329.1:n.109+1923T>C
XM_006711266.3:c.109+1923T>C	XP_006711329.1:n.109+1923T>C
NM_001143674.4:c.109+1923T>C MANE Select	NP_001137146.1:n.109+1923T>C
NR_026550.3:n.264+1923T>C