Canonical Allele Identifier: CA300116387
Gene: MEX3C HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51186670C>T , CM000680.2:g.51186670C>T GRCh38
NC_000018.9:g.48713040C>T , CM000680.1:g.48713040C>T GRCh37
NC_000018.8:g.46967038C>T NCBI36
NG_015801.1:g.16012G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000406189.4:c.755-9094G>A MANE Select ENSP00000385610.3:n.755-9094G>A
ENST00000591040.2:c.-107-9094G>A ENSP00000502049.1:n.-107-9094G>A
ENST00000406189.3:c.755-9094G>A ENSP00000385610.3:n.755-9094G>A
ENST00000591040.1:n.44-9094G>A
ENST00000616921.1:c.245-9094G>A ENSP00000482566.1:n.245-9094G>A
NM_016626.4:c.755-9094G>A NP_057710.3:n.755-9094G>A
NM_016626.5:c.755-9094G>A MANE Select NP_057710.3:n.755-9094G>A